Canonical Allele Identifier: CA1619080578
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271380C= , CM000668.2:g.31271380C= GRCh38
NC_000006.11:g.31239157C= , CM000668.1:g.31239157C= GRCh37
NC_000006.10:g.31347136C= NCBI36
NG_029422.2:g.5752G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-32G= MANE Select ENSP00000365402.5:n.344-32G=
ENST00000376228.9:c.344-32G= ENSP00000365402.5:n.344-32G=
ENST00000376237.8:c.344-49G= ENSP00000365412.4:n.344-49G=
ENST00000383329.7:c.344-32G= ENSP00000372819.3:n.344-32G=
ENST00000415537.1:c.342-32G=
ENST00000484378.1:n.581G=
ENST00000487245.5:n.671G=
ENST00000495835.1:n.533-32G=
NM_002117.5:c.344-32G= NP_002108.4:n.344-32G=
NM_002117.6:c.344-32G= MANE Select NP_002108.4:n.344-32G=