Canonical Allele Identifier: CA1619080476

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271278G= , CM000668.2:g.31271278G=	GRCh38
NC_000006.11:g.31239055G= , CM000668.1:g.31239055G=	GRCh37
NC_000006.10:g.31347034G=	NCBI36
NG_029422.2:g.5854C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.414C= MANE Select	ENSP00000365402.5:p.Asp138=
ENST00000376228.9:c.414C=	ENSP00000365402.5:p.Asp138=
ENST00000376237.8:c.*1C=	ENSP00000365412.4:n.*1C=
ENST00000383329.7:c.414C=	ENSP00000372819.3:p.Asp138=
ENST00000415537.1:c.412C=
ENST00000484378.1:n.683C=
ENST00000487245.5:n.773C=
ENST00000495835.1:n.603C=
NM_002117.5:c.414C=	NP_002108.4:p.Asp138=
NM_002117.6:c.414C= MANE Select	NP_002108.4:p.Asp138=