Canonical Allele Identifier: CA1619079930
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270432G= , CM000668.2:g.31270432G= GRCh38
NC_000006.11:g.31238209G= , CM000668.1:g.31238209G= GRCh37
NC_000006.10:g.31346188G= NCBI36
NG_029422.2:g.6700C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.673C= MANE Select ENSP00000365402.5:p.Leu225=
ENST00000376228.9:c.673C= ENSP00000365402.5:p.Leu225=
ENST00000376237.8:c.*260C= ENSP00000365412.4:n.*260C=
ENST00000383329.7:c.673C= ENSP00000372819.3:p.Leu225=
ENST00000415537.1:c.664+7C=
ENST00000487245.5:n.1032C=
ENST00000495835.1:n.862C=
NM_002117.5:c.673C= NP_002108.4:p.Leu225=
NM_002117.6:c.673C= MANE Select NP_002108.4:p.Leu225=