Canonical Allele Identifier: CA1619080398

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271190G= , CM000668.2:g.31271190G=	GRCh38
NC_000006.11:g.31238967G= , CM000668.1:g.31238967G=	GRCh37
NC_000006.10:g.31346946G=	NCBI36
NG_029422.2:g.5942C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.502C= MANE Select	ENSP00000365402.5:p.Gln168=
ENST00000376228.9:c.502C=	ENSP00000365402.5:p.Gln168=
ENST00000376237.8:c.*89C=	ENSP00000365412.4:n.*89C=
ENST00000383329.7:c.502C=	ENSP00000372819.3:p.Gln168=
ENST00000415537.1:c.500C=
ENST00000484378.1:n.771C=
ENST00000487245.5:n.861C=
ENST00000495835.1:n.691C=
NM_002117.5:c.502C=	NP_002108.4:p.Gln168=
NM_002117.6:c.502C= MANE Select	NP_002108.4:p.Gln168=