Canonical Allele Identifier: CA1619077109
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268820_31268822delinsACG , CM000668.2:g.31268820_31268822delinsACG GRCh38
NC_000006.11:g.31236597_31236599delinsACG , CM000668.1:g.31236597_31236599delinsACG GRCh37
NC_000006.10:g.31344576_31344578delinsACG NCBI36
NG_029422.2:g.8310_8312delinsCGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*347_*349delinsCGT MANE Select ENSP00000365402.5:n.*347_*349delinsCGT
ENST00000376228.9:c.*347_*349delinsCGT ENSP00000365402.5:n.*347_*349delinsCGT
ENST00000376237.8:c.*1035_*1037delinsCGT ENSP00000365412.4:n.*1035_*1037delinsCGT
ENST00000383329.7:c.*347_*349delinsCGT ENSP00000372819.3:n.*347_*349delinsCGT
ENST00000466892.5:n.681_683delinsCGT
ENST00000470363.5:n.1206_1208delinsCGT
ENST00000487245.5:n.1807_1809delinsCGT
NM_002117.5:c.*347_*349delinsCGT NP_002108.4:n.*347_*349delinsCGT
NM_002117.6:c.*347_*349delinsCGT MANE Select NP_002108.4:n.*347_*349delinsCGT