Human (GRCh38.p14)
Description

integrin subunit alpha X [Source:HGNC Symbol;Acc:HGNC:6152]

Gene Synonyms

CD11C

Location
About this transcript

This transcript has 30 exons, is annotated with 65 domains and features, is associated with 14148 variant alleles and maps to 947 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000268296.9ITGAX-20146631163aaENSP00000268296.5
 
Protein coding
CCDS10711P20702 NM_000887.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000562522.2ITGAX-20339901169aaENSP00000454623.1
 
Protein coding
CCDS67014H3BN02 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000562918.5ITGAX-2041521181aaENSP00000483860.1
 
Protein coding
A0A087X131 -GENCODE basicTSL:2
ENST00000571644.1ITGAX-2074382No protein-
 
Retained intron
--TSL:2
ENST00000567409.1ITGAX-2061146No protein-
 
Retained intron
--TSL:1
ENST00000564308.1ITGAX-205544No protein-
 
Retained intron
--TSL:4
ENST00000562138.1ITGAX-202501No protein-
 
Retained intron
--TSL:4
Statistics

Exons: 30, Coding exons: 30, Transcript length: 4,663 bps, Translation length: 1,163 residues

MANE

This MANE Select transcript contains ENSP00000268296 and matches to NM_000887.5 and NP_000878.2

Uniprot

This transcript corresponds to the following Uniprot identifiers: P20702

CCDS

This transcript is a member of the Human CCDS set: CCDS10711

Transcript Support Level (TSL)

TSL:1

Version

ENST00000268296.9

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.