Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

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

Location

Scaffold HSCHR6_MHC_MANN_CTG1: 1,089,454-1,093,611 forward strand.

GRCh38:GL000253.2

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
ENST00000422371.5HLA-G-2361490343aaENSP00000387624.1
 
Protein coding
Q5RJ85 -Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:NA
ENST00000550897.1HLA-G-2421578338aaENSP00000449903.1
 
Protein coding
P17693-1 -GENCODE BasicTSL:NA
ENST00000428952.6HLA-G-2381427338aaENSP00000388176.2
 
Protein coding
P17693-1 -GENCODE BasicTSL:NA
ENST00000426863.6HLA-G-2371127246aaENSP00000392075.2
 
Protein coding
P17693-2 -GENCODE BasicTSL:NA
ENST00000429890.6HLA-G-239851154aaENSP00000401326.2
 
Protein coding
P17693-3 -GENCODE BasicTSL:NA
ENST00000467814.5HLA-G-2411175246aaENSP00000434622.1
 
Nonsense mediated decay
P17693-2 -TSL:NA
ENST00000459768.5HLA-G-2401525No protein-
 
Retained intron
--TSL:NA