Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_DBB_CTG1: 1,089,780-1,093,938 forward strand.

GRCh38:GL000252.2

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
ENST00000420559.5HLA-G-2291490343aaENSP00000397331.1
 
Protein coding
Q5RJ85 -Ensembl CanonicalGENCODE basicTSL:NA
ENST00000546634.1HLA-G-2351578338aaENSP00000447780.1
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000423373.6HLA-G-2301427338aaENSP00000405238.2
 
Protein coding
P17693-1 -GENCODE basicTSL:NA
ENST00000452577.6HLA-G-2311127246aaENSP00000415905.2
 
Protein coding
P17693-2 -GENCODE basicTSL:NA
ENST00000457132.6HLA-G-232851154aaENSP00000410247.2
 
Protein coding
P17693-3 -GENCODE basicTSL:NA
ENST00000469347.5HLA-G-2331175246aaENSP00000437036.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000484755.5HLA-G-2341525No protein-
 
Retained intron
--TSL:NA