Canonical Allele Identifier: CA1619077919
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269469C= , CM000668.2:g.31269469C= GRCh38
NC_000006.11:g.31237246C= , CM000668.1:g.31237246C= GRCh37
NC_000006.10:g.31345225C= NCBI36
NG_029422.2:g.7663G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1048+24G= MANE Select ENSP00000365402.5:n.1048+24G=
ENST00000376228.9:c.1048+24G= ENSP00000365402.5:n.1048+24G=
ENST00000376237.8:c.*635+24G= ENSP00000365412.4:n.*635+24G=
ENST00000383329.7:c.1066+24G= ENSP00000372819.3:n.1066+24G=
ENST00000466892.5:n.198G=
ENST00000470363.5:n.806+24G=
ENST00000487245.5:n.1407+24G=
NM_002117.5:c.1048+24G= NP_002108.4:n.1048+24G=
NM_002117.6:c.1048+24G= MANE Select NP_002108.4:n.1048+24G=