Canonical Allele Identifier: CA2677949756
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269460_31269461insGATA , CM000668.2:g.31269460_31269461insGATA GRCh38
NC_000006.11:g.31237237_31237238insGATA , CM000668.1:g.31237237_31237238insGATA GRCh37
NC_000006.10:g.31345216_31345217insGATA NCBI36
NG_029422.2:g.7671_7672insTATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1048+32_1048+33insTATC MANE Select ENSP00000365402.5:n.1048+32_1048+33insTATC
ENST00000376228.9:c.1048+32_1048+33insTATC ENSP00000365402.5:n.1048+32_1048+33insTATC
ENST00000376237.8:c.*635+32_*635+33insTATC ENSP00000365412.4:n.*635+32_*635+33insTATC
ENST00000383329.7:c.1066+32_1066+33insTATC ENSP00000372819.3:n.1066+32_1066+33insTATC
ENST00000466892.5:n.206_207insTATC
ENST00000470363.5:n.806+32_806+33insTATC
ENST00000487245.5:n.1407+32_1407+33insTATC
NM_002117.5:c.1048+32_1048+33insTATC NP_002108.4:n.1048+32_1048+33insTATC
NM_002117.6:c.1048+32_1048+33insTATC MANE Select NP_002108.4:n.1048+32_1048+33insTATC