Primary_assembly 3R: 23,801,714-23,819,237 reverse strand.
BDGP6.32:AE014297.3
This gene has 5 transcripts (splice variants) and 48 orthologues.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
CG33111-RA | FBtr0084529 | 2552 | 515aa | FBpp0083914 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q9VCH2 | NM_001014646.2 NM_176548 NM_176548.4 NM_206549.4 NP_001014646.1 NP_788725 NP_788725.1 NP_996272.1 | 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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5, |
CG33111-RB | FBtr0084530 | 2432 | 515aa | FBpp0083915 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q9VCH2 | NM_001014646.2 NM_176548.4 NM_206549 NM_206549.4 NP_001014646.1 NP_788725.1 NP_996272 NP_996272.1 | APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5, |
CG33111-RE | FBtr0334893 | 2418 | 353aa | FBpp0306914 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A0B4KHB3 | NM_001275958 NM_001275958.1 NP_001262887 NP_001262887.1 | 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, |
CG33111-RC | FBtr0100312 | 2400 | 515aa | FBpp0099717 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q7YTY2 Q9VCH2 | NM_001014646 NM_001014646.2 NM_176548.4 NM_206549.4 NP_001014646 NP_001014646.1 NP_788725.1 NP_996272.1 | APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5, |
CG33111-RD | FBtr0334892 | 2191 | 338aa | FBpp0306913 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | A0A0B4KGQ7 | NM_001275957 NM_001275957.1 NP_001262886 NP_001262886.1 | 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, |