Canonical Allele Identifier: CA1619078114
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269576_31269577delinsTG , CM000668.2:g.31269576_31269577delinsTG GRCh38
NC_000006.11:g.31237353_31237354delinsTG , CM000668.1:g.31237353_31237354delinsTG GRCh37
NC_000006.10:g.31345332_31345333delinsTG NCBI36
NG_029422.2:g.7555_7556delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-52_1016-51delinsCA MANE Select ENSP00000365402.5:n.1016-52_1016-51delinsCA
ENST00000376228.9:c.1016-52_1016-51delinsCA ENSP00000365402.5:n.1016-52_1016-51delinsCA
ENST00000376237.8:c.*603-52_*603-51delinsCA ENSP00000365412.4:n.*603-52_*603-51delinsCA
ENST00000383329.7:c.1016-34_1016-33delinsCA ENSP00000372819.3:n.1016-34_1016-33delinsCA
ENST00000466892.5:n.90_91delinsCA
ENST00000470363.5:n.722_723delinsCA
ENST00000487245.5:n.1375-52_1375-51delinsCA
NM_002117.5:c.1016-52_1016-51delinsCA NP_002108.4:n.1016-52_1016-51delinsCA
NM_002117.6:c.1016-52_1016-51delinsCA MANE Select NP_002108.4:n.1016-52_1016-51delinsCA
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