Canonical Allele Identifier: CA1619080465

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271266G= , CM000668.2:g.31271266G=	GRCh38
NC_000006.11:g.31239043G= , CM000668.1:g.31239043G=	GRCh37
NC_000006.10:g.31347022G=	NCBI36
NG_029422.2:g.5866C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.426C= MANE Select	ENSP00000365402.5:p.Tyr142=
ENST00000376228.9:c.426C=	ENSP00000365402.5:p.Tyr142=
ENST00000376237.8:c.*13C=	ENSP00000365412.4:n.*13C=
ENST00000383329.7:c.426C=	ENSP00000372819.3:p.Tyr142=
ENST00000415537.1:c.424C=
ENST00000484378.1:n.695C=
ENST00000487245.5:n.785C=
ENST00000495835.1:n.615C=
NM_002117.5:c.426C=	NP_002108.4:p.Tyr142=
NM_002117.6:c.426C= MANE Select	NP_002108.4:p.Tyr142=