Canonical Allele Identifier: CA2677949757
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269462_31269463insTAAG , CM000668.2:g.31269462_31269463insTAAG GRCh38
NC_000006.11:g.31237239_31237240insTAAG , CM000668.1:g.31237239_31237240insTAAG GRCh37
NC_000006.10:g.31345218_31345219insTAAG NCBI36
NG_029422.2:g.7671_7672insTACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1048+32_1048+33insTACT MANE Select ENSP00000365402.5:n.1048+32_1048+33insTACT
ENST00000376228.9:c.1048+32_1048+33insTACT ENSP00000365402.5:n.1048+32_1048+33insTACT
ENST00000376237.8:c.*635+32_*635+33insTACT ENSP00000365412.4:n.*635+32_*635+33insTACT
ENST00000383329.7:c.1066+32_1066+33insTACT ENSP00000372819.3:n.1066+32_1066+33insTACT
ENST00000466892.5:n.206_207insTACT
ENST00000470363.5:n.806+32_806+33insTACT
ENST00000487245.5:n.1407+32_1407+33insTACT
NM_002117.5:c.1048+32_1048+33insTACT NP_002108.4:n.1048+32_1048+33insTACT
NM_002117.6:c.1048+32_1048+33insTACT MANE Select NP_002108.4:n.1048+32_1048+33insTACT