Canonical Allele Identifier: CA1619080765

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271647G= , CM000668.2:g.31271647G=	GRCh38
NC_000006.11:g.31239424G= , CM000668.1:g.31239424G=	GRCh37
NC_000006.10:g.31347403G=	NCBI36
NG_029422.2:g.5485C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.295C= MANE Select	ENSP00000365402.5:p.Arg99=
ENST00000376228.9:c.295C=	ENSP00000365402.5:p.Arg99=
ENST00000376237.8:c.295C=	ENSP00000365412.4:p.Arg99=
ENST00000383329.7:c.295C=	ENSP00000372819.3:p.Arg99=
ENST00000415537.1:c.293C=
ENST00000484378.1:n.314C=
ENST00000487245.5:n.404C=
ENST00000495835.1:n.484C=
NM_002117.5:c.295C=	NP_002108.4:p.Arg99=
NM_002117.6:c.295C= MANE Select	NP_002108.4:p.Arg99=