Primary_assembly 2R: 14,261,206-14,267,919 reverse strand.
BDGP6.32:AE013599.5
This gene has 3 transcripts (splice variants) and 66 orthologues.
Name | Transcript ID | bp | Protein | Translation ID | Biotype | UniProt | RefSeq | Flags |
---|---|---|---|---|---|---|---|---|
CG8547-RC | FBtr0301203 | 2676 | 618aa | FBpp0290421 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q0E980 | NM_001299486.1 NM_137103 NM_137103.4 NM_166044.3 NP_001286415.1 NP_610947 NP_610947.3 NP_725373.2 | 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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, |
CG8547-RE | FBtr0339968 | 2640 | 618aa | FBpp0308989 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q0E980 Q961R5 | NM_001299486 NM_001299486.1 NM_137103.4 NM_166044.3 NP_001286415 NP_001286415.1 NP_610947.3 NP_725373.2 | APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, |
CG8547-RD | FBtr0301204 | 2614 | 618aa | FBpp0290422 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | Q0E980 | NM_001299486.1 NM_137103.4 NM_166044 NM_166044.3 NP_001286415.1 NP_610947.3 NP_725373 NP_725373.2 | APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1, |