Canonical Allele Identifier: CA1619077734

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269361T= , CM000668.2:g.31269361T=	GRCh38
NC_000006.11:g.31237138T= , CM000668.1:g.31237138T=	GRCh37
NC_000006.10:g.31345117T=	NCBI36
NG_029422.2:g.7771A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1073A= MANE Select	ENSP00000365402.5:p.Asp358=
ENST00000376228.9:c.1073A=	ENSP00000365402.5:p.Asp358=
ENST00000376237.8:c.*660A=	ENSP00000365412.4:n.*660A=
ENST00000383329.7:c.1091A=	ENSP00000372819.3:p.Asp364=
ENST00000466892.5:n.306A=
ENST00000470363.5:n.831A=
ENST00000487245.5:n.1432A=
NM_002117.5:c.1073A=	NP_002108.4:p.Asp358=
NM_002117.6:c.1073A= MANE Select	NP_002108.4:p.Asp358=