Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_QBL_CTG1: 1,089,733-1,093,907 forward strand.

GRCh38:GL000255.2

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
ENST00000400682.5HLA-G-2111506343aaENSP00000383521.1
 
Protein coding
Q5RJ85 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000553052.2HLA-G-2141582338aaENSP00000449291.1
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000383621.8HLA-G-2081443338aaENSP00000373116.4
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000383623.8HLA-G-2101143246aaENSP00000373118.4
 
Protein coding
P17693-2 -GENCODE basicTSL:NA
ENST00000383622.8HLA-G-209867154aaENSP00000373117.4
 
Protein coding
P17693-3 -GENCODE basicTSL:NA
ENST00000469472.5HLA-G-2121191246aaENSP00000432220.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000491141.5HLA-G-2131541No protein-
 
Retained intron
--TSL:NA