Human (GRCh38.p14)
Description

NSF attachment protein gamma [Source:HGNC Symbol;Acc:HGNC:7642]

Location
About this transcript

This transcript has 12 exons, is annotated with 9 domains and features, is associated with 12091 variant alleles and maps to 541 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000322897.11NAPG-2013559312aaENSP00000324628.6
 
Protein coding
CCDS45827Q99747-1 NM_003826.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000582472.3NAPG-205694177aaENSP00000463018.3
 
Protein coding
J3KTJ6 -TSL:5CDS 3' incomplete
ENST00000580483.5NAPG-203151618aaENSP00000464496.1
 
Nonsense mediated decay
J3QS28 -TSL:3
ENST00000580224.5NAPG-202124522aaENSP00000463265.1
 
Nonsense mediated decay
J3QKW4 -TSL:2
ENST00000583367.1NAPG-2073860No protein-
 
Retained intron
--TSL:2
ENST00000582978.5NAPG-206887No protein-
 
Retained intron
--TSL:2
ENST00000580746.1NAPG-204743No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 12, Coding exons: 12, Transcript length: 3,559 bps, Translation length: 312 residues

MANE

This MANE Select transcript contains ENSP00000324628 and matches to NM_003826.3 and NP_003817.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q99747

CCDS

This transcript is a member of the Human CCDS set: CCDS45827

Transcript Support Level (TSL)

TSL:1

Version

ENST00000322897.11

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.