Canonical Allele Identifier: CA1619080494

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271298G= , CM000668.2:g.31271298G=	GRCh38
NC_000006.11:g.31239075G= , CM000668.1:g.31239075G=	GRCh37
NC_000006.10:g.31347054G=	NCBI36
NG_029422.2:g.5834C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.394C= MANE Select	ENSP00000365402.5:p.Arg132=
ENST00000376228.9:c.394C=	ENSP00000365402.5:p.Arg132=
ENST00000376237.8:c.377C=	ENSP00000365412.4:p.Ala126=
ENST00000383329.7:c.394C=	ENSP00000372819.3:p.Arg132=
ENST00000415537.1:c.392C=
ENST00000484378.1:n.663C=
ENST00000487245.5:n.753C=
ENST00000495835.1:n.583C=
NM_002117.5:c.394C=	NP_002108.4:p.Arg132=
NM_002117.6:c.394C= MANE Select	NP_002108.4:p.Arg132=