Canonical Allele Identifier: CA1619080135
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270759G= , CM000668.2:g.31270759G= GRCh38
NC_000006.11:g.31238536G= , CM000668.1:g.31238536G= GRCh37
NC_000006.10:g.31346515G= NCBI36
NG_029422.2:g.6373C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-274C= MANE Select ENSP00000365402.5:n.620-274C=
ENST00000376228.9:c.620-274C= ENSP00000365402.5:n.620-274C=
ENST00000376237.8:c.*207-274C= ENSP00000365412.4:n.*207-274C=
ENST00000383329.7:c.620-274C= ENSP00000372819.3:n.620-274C=
ENST00000415537.1:c.618-274C=
ENST00000487245.5:n.979-274C=
ENST00000495835.1:n.809-274C=
NM_002117.5:c.620-274C= NP_002108.4:n.620-274C=
NM_002117.6:c.620-274C= MANE Select NP_002108.4:n.620-274C=
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