Canonical Allele Identifier: CA1087451185
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269576_31269577del , CM000668.2:g.31269576_31269577del GRCh38
NC_000006.11:g.31237353_31237354del , CM000668.1:g.31237353_31237354del GRCh37
NC_000006.10:g.31345332_31345333del NCBI36
NG_029422.2:g.7557_7558del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-50_1016-49del MANE Select ENSP00000365402.5:n.1016-50_1016-49del
ENST00000376228.9:c.1016-50_1016-49del ENSP00000365402.5:n.1016-50_1016-49del
ENST00000376237.8:c.*603-50_*603-49del ENSP00000365412.4:n.*603-50_*603-49del
ENST00000383329.7:c.1016-32_1016-31del ENSP00000372819.3:n.1016-32_1016-31del
ENST00000466892.5:n.92_93del
ENST00000470363.5:n.724_725del
ENST00000487245.5:n.1375-50_1375-49del
NM_002117.5:c.1016-50_1016-49del NP_002108.4:n.1016-50_1016-49del
NM_002117.6:c.1016-50_1016-49del MANE Select NP_002108.4:n.1016-50_1016-49del