Canonical Allele Identifier: CA1087424362
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31270676-A-AAG
gnomAD v4: 6-31270676-A-AAG
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270676_31270677insAG , CM000668.2:g.31270676_31270677insAG GRCh38
NC_000006.11:g.31238453_31238454insAG , CM000668.1:g.31238453_31238454insAG GRCh37
NC_000006.10:g.31346432_31346433insAG NCBI36
NG_029422.2:g.6455_6456insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-192_620-191insCT MANE Select ENSP00000365402.5:n.620-192_620-191insCT
ENST00000376228.9:c.620-192_620-191insCT ENSP00000365402.5:n.620-192_620-191insCT
ENST00000376237.8:c.*207-192_*207-191insCT ENSP00000365412.4:n.*207-192_*207-191insCT
ENST00000383329.7:c.620-192_620-191insCT ENSP00000372819.3:n.620-192_620-191insCT
ENST00000415537.1:c.618-192_618-191insCT
ENST00000487245.5:n.979-192_979-191insCT
ENST00000495835.1:n.809-192_809-191insCT
NM_002117.5:c.620-192_620-191insCT NP_002108.4:n.620-192_620-191insCT
NM_002117.6:c.620-192_620-191insCT MANE Select NP_002108.4:n.620-192_620-191insCT
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