Canonical Allele Identifier: CA1619080391

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271184T= , CM000668.2:g.31271184T=	GRCh38
NC_000006.11:g.31238961T= , CM000668.1:g.31238961T=	GRCh37
NC_000006.10:g.31346940T=	NCBI36
NG_029422.2:g.5948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.508A= MANE Select	ENSP00000365402.5:p.Lys170=
ENST00000376228.9:c.508A=	ENSP00000365402.5:p.Lys170=
ENST00000376237.8:c.*95A=	ENSP00000365412.4:n.*95A=
ENST00000383329.7:c.508A=	ENSP00000372819.3:p.Lys170=
ENST00000415537.1:c.506A=
ENST00000484378.1:n.777A=
ENST00000487245.5:n.867A=
ENST00000495835.1:n.697A=
NM_002117.5:c.508A=	NP_002108.4:p.Lys170=
NM_002117.6:c.508A= MANE Select	NP_002108.4:p.Lys170=