Canonical Allele Identifier: CA2504782125
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269783_31269784insAA , CM000668.2:g.31269783_31269784insAA GRCh38
NC_000006.11:g.31237560_31237561insAA , CM000668.1:g.31237560_31237561insAA GRCh37
NC_000006.10:g.31345539_31345540insAA NCBI36
NG_029422.2:g.7349_7350insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+183_1015+184insTT MANE Select ENSP00000365402.5:n.1015+183_1015+184insTT
ENST00000376228.9:c.1015+183_1015+184insTT ENSP00000365402.5:n.1015+183_1015+184insTT
ENST00000376237.8:c.*602+183_*602+184insTT ENSP00000365412.4:n.*602+183_*602+184insTT
ENST00000383329.7:c.1015+183_1015+184insTT ENSP00000372819.3:n.1015+183_1015+184insTT
ENST00000470363.5:n.516_517insTT
ENST00000487245.5:n.1374+183_1374+184insTT
NM_002117.5:c.1015+183_1015+184insTT NP_002108.4:n.1015+183_1015+184insTT
NM_002117.6:c.1015+183_1015+184insTT MANE Select NP_002108.4:n.1015+183_1015+184insTT
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