Canonical Allele Identifier: CA1087448854
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31268871-T-TTG
gnomAD v4: 6-31268871-T-TTG
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268872_31268873insGT , CM000668.2:g.31268872_31268873insGT GRCh38
NC_000006.11:g.31236649_31236650insGT , CM000668.1:g.31236649_31236650insGT GRCh37
NC_000006.10:g.31344628_31344629insGT NCBI36
NG_029422.2:g.8260_8261insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*297_*298insCA MANE Select ENSP00000365402.5:n.*297_*298insCA
ENST00000376228.9:c.*297_*298insCA ENSP00000365402.5:n.*297_*298insCA
ENST00000376237.8:c.*985_*986insCA ENSP00000365412.4:n.*985_*986insCA
ENST00000383329.7:c.*297_*298insCA ENSP00000372819.3:n.*297_*298insCA
ENST00000466892.5:n.631_632insCA
ENST00000470363.5:n.1156_1157insCA
ENST00000487245.5:n.1757_1758insCA
NM_002117.5:c.*297_*298insCA NP_002108.4:n.*297_*298insCA
NM_002117.6:c.*297_*298insCA MANE Select NP_002108.4:n.*297_*298insCA
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