Canonical Allele Identifier: CA1087451200
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269577_31269578insCAA , CM000668.2:g.31269577_31269578insCAA GRCh38
NC_000006.11:g.31237354_31237355insCAA , CM000668.1:g.31237354_31237355insCAA GRCh37
NC_000006.10:g.31345333_31345334insCAA NCBI36
NG_029422.2:g.7554_7555insTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-53_1016-52insTTG MANE Select ENSP00000365402.5:n.1016-53_1016-52insTTG
ENST00000376228.9:c.1016-53_1016-52insTTG ENSP00000365402.5:n.1016-53_1016-52insTTG
ENST00000376237.8:c.*603-53_*603-52insTTG ENSP00000365412.4:n.*603-53_*603-52insTTG
ENST00000383329.7:c.1016-35_1016-34insTTG ENSP00000372819.3:n.1016-35_1016-34insTTG
ENST00000466892.5:n.89_90insTTG
ENST00000470363.5:n.721_722insTTG
ENST00000487245.5:n.1375-53_1375-52insTTG
NM_002117.5:c.1016-53_1016-52insTTG NP_002108.4:n.1016-53_1016-52insTTG
NM_002117.6:c.1016-53_1016-52insTTG MANE Select NP_002108.4:n.1016-53_1016-52insTTG