Human (GRCh38.p14)
Description

sorting nexin 7 [Source:HGNC Symbol;Acc:HGNC:14971]

Location
About this transcript

This transcript has 9 exons, is annotated with 11 domains and features, is associated with 41145 variant alleles and maps to 538 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000306121.8SNX7-2011736451aaENSP00000304429.3
 
Protein coding
CCDS755Q9UNH6-3 NM_015976.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000529992.5SNX7-2051589396aaENSP00000434731.1
 
Protein coding
CCDS756E9PNL2 -GENCODE basicTSL:2
ENST00000454199.1SNX7-202497108aaENSP00000388266.1
 
Protein coding
B7ZC83 -TSL:4CDS 3' incomplete
ENST00000528824.1SNX7-204156236aaENSP00000435172.1
 
Nonsense mediated decay
E9PLE1 -TSL:1
ENST00000473868.5SNX7-203253No protein-
 
Protein coding CDS not defined
--TSL:3
Statistics

Exons: 9, Coding exons: 9, Transcript length: 1,736 bps, Translation length: 451 residues

MANE

This MANE Select transcript contains ENSP00000304429 and matches to NM_015976.5 and NP_057060.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UNH6

CCDS

This transcript is a member of the Human CCDS set: CCDS755

Transcript Support Level (TSL)

TSL:1

Version

ENST00000306121.8

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.