Canonical Allele Identifier: CA1619077893

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269453A= , CM000668.2:g.31269453A=	GRCh38
NC_000006.11:g.31237230A= , CM000668.1:g.31237230A=	GRCh37
NC_000006.10:g.31345209A=	NCBI36
NG_029422.2:g.7679T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+40T= MANE Select	ENSP00000365402.5:n.1048+40T=
ENST00000376228.9:c.1048+40T=	ENSP00000365402.5:n.1048+40T=
ENST00000376237.8:c.*635+40T=	ENSP00000365412.4:n.*635+40T=
ENST00000383329.7:c.1066+40T=	ENSP00000372819.3:n.1066+40T=
ENST00000466892.5:n.214T=
ENST00000470363.5:n.806+40T=
ENST00000487245.5:n.1407+40T=
NM_002117.5:c.1048+40T=	NP_002108.4:n.1048+40T=
NM_002117.6:c.1048+40T= MANE Select	NP_002108.4:n.1048+40T=