Canonical Allele Identifier: CA136860946
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9281298

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268824_31268825insC , CM000668.2:g.31268824_31268825insC GRCh38
NC_000006.11:g.31236601_31236602insC , CM000668.1:g.31236601_31236602insC GRCh37
NC_000006.10:g.31344580_31344581insC NCBI36
NG_029422.2:g.8307_8308insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*344_*345insG MANE Select ENSP00000365402.5:n.*344_*345insG
ENST00000376228.9:c.*344_*345insG ENSP00000365402.5:n.*344_*345insG
ENST00000376237.8:c.*1032_*1033insG ENSP00000365412.4:n.*1032_*1033insG
ENST00000383329.7:c.*344_*345insG ENSP00000372819.3:n.*344_*345insG
ENST00000466892.5:n.678_679insG
ENST00000470363.5:n.1203_1204insG
ENST00000487245.5:n.1804_1805insG
NM_002117.5:c.*344_*345insG NP_002108.4:n.*344_*345insG
NM_002117.6:c.*344_*345insG MANE Select NP_002108.4:n.*344_*345insG