Canonical Allele Identifier: CA1619078305
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269711_31269714delinsTTAG , CM000668.2:g.31269711_31269714delinsTTAG GRCh38
NC_000006.11:g.31237488_31237491delinsTTAG , CM000668.1:g.31237488_31237491delinsTTAG GRCh37
NC_000006.10:g.31345467_31345470delinsTTAG NCBI36
NG_029422.2:g.7418_7421delinsCTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-189_1016-186delinsCTAA MANE Select ENSP00000365402.5:n.1016-189_1016-186delinsCTAA
ENST00000376228.9:c.1016-189_1016-186delinsCTAA ENSP00000365402.5:n.1016-189_1016-186delinsCTAA
ENST00000376237.8:c.*603-189_*603-186delinsCTAA ENSP00000365412.4:n.*603-189_*603-186delinsCTAA
ENST00000383329.7:c.1016-171_1016-168delinsCTAA ENSP00000372819.3:n.1016-171_1016-168delinsCTAA
ENST00000470363.5:n.585_588delinsCTAA
ENST00000487245.5:n.1375-189_1375-186delinsCTAA
NM_002117.5:c.1016-189_1016-186delinsCTAA NP_002108.4:n.1016-189_1016-186delinsCTAA
NM_002117.6:c.1016-189_1016-186delinsCTAA MANE Select NP_002108.4:n.1016-189_1016-186delinsCTAA
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