Canonical Allele Identifier: CA136860935
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs386698952

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268822_31268824delinsCTC , CM000668.2:g.31268822_31268824delinsCTC GRCh38
NC_000006.11:g.31236599_31236601delinsCTC , CM000668.1:g.31236599_31236601delinsCTC GRCh37
NC_000006.10:g.31344578_31344580delinsCTC NCBI36
NG_029422.2:g.8308_8310delinsGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*345_*347delinsGAG MANE Select ENSP00000365402.5:n.*345_*347delinsGAG
ENST00000376228.9:c.*345_*347delinsGAG ENSP00000365402.5:n.*345_*347delinsGAG
ENST00000376237.8:c.*1033_*1035delinsGAG ENSP00000365412.4:n.*1033_*1035delinsGAG
ENST00000383329.7:c.*345_*347delinsGAG ENSP00000372819.3:n.*345_*347delinsGAG
ENST00000466892.5:n.679_681delinsGAG
ENST00000470363.5:n.1204_1206delinsGAG
ENST00000487245.5:n.1805_1807delinsGAG
NM_002117.5:c.*345_*347delinsGAG NP_002108.4:n.*345_*347delinsGAG
NM_002117.6:c.*345_*347delinsGAG MANE Select NP_002108.4:n.*345_*347delinsGAG