Human (GRCh38.p14)
Description

major histocompatibility complex, class I, G [Source:HGNC Symbol;Acc:HGNC:4964]

Location

Scaffold HSCHR6_MHC_MCF_CTG1: 1,089,438-1,093,596 forward strand.

GRCh38:GL000254.2

View this gene on the primary assembly.

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000450984.5HLA-G-2461490343aaENSP00000409132.1
 
Protein coding
Q5RJ85 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000547931.1HLA-G-2491578338aaENSP00000448363.1
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000449127.6HLA-G-2451427338aaENSP00000408773.2
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000412263.6HLA-G-2431127246aaENSP00000397733.2
 
Protein coding
P17693-2 -GENCODE basicTSL:NA
ENST00000415687.6HLA-G-244851154aaENSP00000389969.2
 
Protein coding
P17693-3 -GENCODE basicTSL:NA
ENST00000466488.5HLA-G-2471175246aaENSP00000433426.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000494247.5HLA-G-2481525No protein-
 
Retained intron
--TSL:NA