Canonical Allele Identifier: CA2677949220
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268989_31268990insAT , CM000668.2:g.31268989_31268990insAT GRCh38
NC_000006.11:g.31236766_31236767insAT , CM000668.1:g.31236766_31236767insAT GRCh37
NC_000006.10:g.31344745_31344746insAT NCBI36
NG_029422.2:g.8143_8144insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*180_*181insTA MANE Select ENSP00000365402.5:n.*180_*181insTA
ENST00000376228.9:c.*180_*181insTA ENSP00000365402.5:n.*180_*181insTA
ENST00000376237.8:c.*868_*869insTA ENSP00000365412.4:n.*868_*869insTA
ENST00000383329.7:c.*180_*181insTA ENSP00000372819.3:n.*180_*181insTA
ENST00000466892.5:n.514_515insTA
ENST00000470363.5:n.1039_1040insTA
ENST00000487245.5:n.1640_1641insTA
NM_002117.5:c.*180_*181insTA NP_002108.4:n.*180_*181insTA
NM_002117.6:c.*180_*181insTA MANE Select NP_002108.4:n.*180_*181insTA