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Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_COX_CTG1: 1,310,529-1,314,698 forward strand.

GRCh38:GL000251.2

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
ENST00000400665.5HLA-G-2151497343aaENSP00000383506.1
 
Protein coding
Q5RJ85 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:NA
ENST00000546545.2HLA-G-2211582338aaENSP00000447762.1
 
Protein coding
P17693-1 -GENCODE BasicTSL:NA
ENST00000444098.6HLA-G-2161434338aaENSP00000398200.2
 
Protein coding
P17693-1 -GENCODE BasicTSL:NA
ENST00000452715.6HLA-G-2181134246aaENSP00000390678.2
 
Protein coding
P17693-2 -GENCODE BasicTSL:NA
ENST00000445373.6HLA-G-217858154aaENSP00000416408.2
 
Protein coding
P17693-3 -GENCODE BasicTSL:NA
ENST00000486553.5HLA-G-2201182246aaENSP00000432239.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000478108.5HLA-G-2191532No protein-
 
Retained intron
--TSL:NA