Human (GRCh38.p14)
Description

sorting nexin 15 [Source:HGNC Symbol;Acc:HGNC:14978]

Location
About this transcript

This transcript has 7 exons, is annotated with 11 domains and features, is associated with 5702 variant alleles and maps to 498 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377244.8SNX15-2021908342aaENSP00000366452.3
 
Protein coding
CCDS8089Q9NRS6-1 NM_013306.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000352068.5SNX15-201771256aaENSP00000316410.5
 
Protein coding
CCDS8090Q9NRS6-2 -GENCODE basicTSL:5
ENST00000534637.5SNX15-207704217aaENSP00000437277.1
 
Protein coding
E9PMW6 -TSL:5CDS 3' incomplete
ENST00000524831.5SNX15-203627192aaENSP00000431690.1
 
Protein coding
E9PK26 -TSL:5CDS 3' incomplete
ENST00000525648.1SNX15-20431266aaENSP00000436023.1
 
Protein coding
E9PR81 -TSL:3CDS 3' incomplete
ENST00000529673.5SNX15-206573114aaENSP00000434778.1
 
Nonsense mediated decay
E9PNI5 -TSL:3
ENST00000526702.1SNX15-2054713No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 771 bps, Translation length: 256 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9NRS6

CCDS

This transcript is a member of the Human CCDS set: CCDS8090

Transcript Support Level (TSL)

TSL:5

Version

ENST00000352068.5

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.