Canonical Allele Identifier: CA136861030
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs796393201

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268907_31268910delinsGTA , CM000668.2:g.31268907_31268910delinsGTA GRCh38
NC_000006.11:g.31236684_31236687delinsGTA , CM000668.1:g.31236684_31236687delinsGTA GRCh37
NC_000006.10:g.31344663_31344666delinsGTA NCBI36
NG_029422.2:g.8222_8225delinsTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*259_*262delinsTAC MANE Select ENSP00000365402.5:n.*259_*262delinsTAC
ENST00000376228.9:c.*259_*262delinsTAC ENSP00000365402.5:n.*259_*262delinsTAC
ENST00000376237.8:c.*947_*950delinsTAC ENSP00000365412.4:n.*947_*950delinsTAC
ENST00000383329.7:c.*259_*262delinsTAC ENSP00000372819.3:n.*259_*262delinsTAC
ENST00000466892.5:n.593_596delinsTAC
ENST00000470363.5:n.1118_1121delinsTAC
ENST00000487245.5:n.1719_1722delinsTAC
NM_002117.5:c.*259_*262delinsTAC NP_002108.4:n.*259_*262delinsTAC
NM_002117.6:c.*259_*262delinsTAC MANE Select NP_002108.4:n.*259_*262delinsTAC