Canonical Allele Identifier: CA1619080497

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271301C= , CM000668.2:g.31271301C=	GRCh38
NC_000006.11:g.31239078C= , CM000668.1:g.31239078C=	GRCh37
NC_000006.10:g.31347057C=	NCBI36
NG_029422.2:g.5831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.391G= MANE Select	ENSP00000365402.5:p.Gly131=
ENST00000376228.9:c.391G=	ENSP00000365402.5:p.Gly131=
ENST00000376237.8:c.374G=	ENSP00000365412.4:p.Arg125=
ENST00000383329.7:c.391G=	ENSP00000372819.3:p.Gly131=
ENST00000415537.1:c.389G=
ENST00000484378.1:n.660G=
ENST00000487245.5:n.750G=
ENST00000495835.1:n.580G=
NM_002117.5:c.391G=	NP_002108.4:p.Gly131=
NM_002117.6:c.391G= MANE Select	NP_002108.4:p.Gly131=