Human (GRCh38.p14)
Description

sorting nexin 22 [Source:HGNC Symbol;Acc:HGNC:16315]

Gene Synonyms

FLJ13952

Location
About this transcript

This transcript has 7 exons, is annotated with 10 domains and features, is associated with 3351 variant alleles and maps to 482 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000325881.9SNX22-2013600193aaENSP00000323435.4
 
Protein coding
CCDS10190Q96L94-1 NM_024798.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000558466.5SNX22-2031353120aaENSP00000452692.1
 
Nonsense mediated decay
Q96L94-2 -TSL:5
ENST00000557789.5SNX22-2023713No protein-
 
Retained intron
--TSL:5
ENST00000560997.1SNX22-2063367No protein-
 
Retained intron
--TSL:1
ENST00000561334.1SNX22-2072789No protein-
 
Retained intron
--TSL:2
ENST00000560945.1SNX22-2051807No protein-
 
Retained intron
--TSL:1
ENST00000560607.5SNX22-2041182No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 7, Coding exons: 7, Transcript length: 3,600 bps, Translation length: 193 residues

MANE

This MANE Select transcript contains ENSP00000323435 and matches to NM_024798.3 and NP_079074.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96L94

CCDS

This transcript is a member of the Human CCDS set: CCDS10190

Transcript Support Level (TSL)

TSL:1

Version

ENST00000325881.9

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.