Canonical Allele Identifier: CA1619079782

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270352G= , CM000668.2:g.31270352G=	GRCh38
NC_000006.11:g.31238129G= , CM000668.1:g.31238129G=	GRCh37
NC_000006.10:g.31346108G=	NCBI36
NG_029422.2:g.6780C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.753C= MANE Select	ENSP00000365402.5:p.Asp251=
ENST00000376228.9:c.753C=	ENSP00000365402.5:p.Asp251=
ENST00000376237.8:c.*340C=	ENSP00000365412.4:n.*340C=
ENST00000383329.7:c.753C=	ENSP00000372819.3:p.Asp251=
ENST00000415537.1:c.665-21C=
ENST00000470363.5:n.71C=
ENST00000487245.5:n.1112C=
ENST00000495835.1:n.942C=
NM_002117.5:c.753C=	NP_002108.4:p.Asp251=
NM_002117.6:c.753C= MANE Select	NP_002108.4:p.Asp251=