Canonical Allele Identifier: CA1619077112
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268821_31268822delinsCG , CM000668.2:g.31268821_31268822delinsCG GRCh38
NC_000006.11:g.31236598_31236599delinsCG , CM000668.1:g.31236598_31236599delinsCG GRCh37
NC_000006.10:g.31344577_31344578delinsCG NCBI36
NG_029422.2:g.8310_8311delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*347_*348delinsCG MANE Select ENSP00000365402.5:n.*347_*348delinsCG
ENST00000376228.9:c.*347_*348delinsCG ENSP00000365402.5:n.*347_*348delinsCG
ENST00000376237.8:c.*1035_*1036delinsCG ENSP00000365412.4:n.*1035_*1036delinsCG
ENST00000383329.7:c.*347_*348delinsCG ENSP00000372819.3:n.*347_*348delinsCG
ENST00000466892.5:n.681_682delinsCG
ENST00000470363.5:n.1206_1207delinsCG
ENST00000487245.5:n.1807_1808delinsCG
NM_002117.5:c.*347_*348delinsCG NP_002108.4:n.*347_*348delinsCG
NM_002117.6:c.*347_*348delinsCG MANE Select NP_002108.4:n.*347_*348delinsCG
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