Canonical Allele Identifier: CA1619079735

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270331C= , CM000668.2:g.31270331C=	GRCh38
NC_000006.11:g.31238108C= , CM000668.1:g.31238108C=	GRCh37
NC_000006.10:g.31346087C=	NCBI36
NG_029422.2:g.6801G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.774G= MANE Select	ENSP00000365402.5:p.Arg258=
ENST00000376228.9:c.774G=	ENSP00000365402.5:p.Arg258=
ENST00000376237.8:c.*361G=	ENSP00000365412.4:n.*361G=
ENST00000383329.7:c.774G=	ENSP00000372819.3:p.Arg258=
ENST00000415537.1:c.665G=
ENST00000470363.5:n.92G=
ENST00000487245.5:n.1133G=
ENST00000495835.1:n.963G=
NM_002117.5:c.774G=	NP_002108.4:p.Arg258=
NM_002117.6:c.774G= MANE Select	NP_002108.4:p.Arg258=