Canonical Allele Identifier: CA1619077758

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269377T= , CM000668.2:g.31269377T=	GRCh38
NC_000006.11:g.31237154T= , CM000668.1:g.31237154T=	GRCh37
NC_000006.10:g.31345133T=	NCBI36
NG_029422.2:g.7755A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1057A= MANE Select	ENSP00000365402.5:p.Ser353=
ENST00000376228.9:c.1057A=	ENSP00000365402.5:p.Ser353=
ENST00000376237.8:c.*644A=	ENSP00000365412.4:n.*644A=
ENST00000383329.7:c.1075A=	ENSP00000372819.3:p.Ser359=
ENST00000466892.5:n.290A=
ENST00000470363.5:n.815A=
ENST00000487245.5:n.1416A=
NM_002117.5:c.1057A=	NP_002108.4:p.Ser353=
NM_002117.6:c.1057A= MANE Select	NP_002108.4:p.Ser353=