Human (GRCh38.p14)
Description

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

Location

Chromosome 6: 29,826,967-29,831,125 forward strand.

GRCh38:CM000668.2

View alleles of this gene on alternative sequences

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele, 130 orthologues, 22 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000360323.11HLA-G-2011319338aaENSP00000353472.6
 
Protein coding
CCDS4668P17693-1 NM_001384290.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2TSL:NA
ENST00000376828.6HLA-G-2041490343aaENSP00000366024.2
 
Protein coding
CCDS87380Q5RJ85 -GENCODE basicAPPRIS ALT2TSL:NA
ENST00000376818.7HLA-G-2031127246aaENSP00000366014.3
 
Protein coding
P17693-2 -GENCODE basicTSL:NA
ENST00000376815.3HLA-G-202851154aaENSP00000366011.3
 
Protein coding
P17693-3 -GENCODE basicTSL:NA
ENST00000478519.5HLA-G-2071175246aaENSP00000436375.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000478355.5HLA-G-2061525No protein-
 
Retained intron
--TSL:NA
ENST00000428701.6HLA-G-2051032No protein-
 
Retained intron
--TSL:NA