taiman
Primary_assembly 2L: 9,166,778-9,247,186 forward strand.
This transcript has 14 exons and is annotated with 92 domains and features.
This transcript is a product of gene FBgn0041092 Show transcript tableHide transcript table
| Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
|---|---|---|---|---|---|---|---|---|
| tai-RG | FBtr0304974 | 11378 | 2047aa | FBpp0293513 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | M9ND53 Q9GS19 | - | A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2, |
| tai-RF | FBtr0303873 | 10859 | 1918aa | FBpp0292876 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | C4IXY4 M9MRG5 Q9GS19 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
| tai-RD | FBtr0303871 | 8290 | 2026aa | FBpp0292874 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q9VLD9 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
| tai-RC | FBtr0303870 | 8158 | 2026aa | FBpp0292873 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q9VLD9 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
| tai-RE | FBtr0303872 | 8125 | 2014aa | FBpp0292875 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | C4IXY4 M9MRJ8 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
| tai-RH | FBtr0333405 | 7966 | 1918aa | FBpp0305597 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | M9MRG5 | - | APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2, |
![[RSS logo]](/i/rss_icon_16.png "Ensembl blog"){kind=icon}
![[twitter logo]](/i/twitter.png "Follow us on Twitter!")
