Canonical Allele Identifier: CA1619077142
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268905_31268906delinsAC , CM000668.2:g.31268905_31268906delinsAC GRCh38
NC_000006.11:g.31236682_31236683delinsAC , CM000668.1:g.31236682_31236683delinsAC GRCh37
NC_000006.10:g.31344661_31344662delinsAC NCBI36
NG_029422.2:g.8226_8227delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*263_*264delinsGT MANE Select ENSP00000365402.5:n.*263_*264delinsGT
ENST00000376228.9:c.*263_*264delinsGT ENSP00000365402.5:n.*263_*264delinsGT
ENST00000376237.8:c.*951_*952delinsGT ENSP00000365412.4:n.*951_*952delinsGT
ENST00000383329.7:c.*263_*264delinsGT ENSP00000372819.3:n.*263_*264delinsGT
ENST00000466892.5:n.597_598delinsGT
ENST00000470363.5:n.1122_1123delinsGT
ENST00000487245.5:n.1723_1724delinsGT
NM_002117.5:c.*263_*264delinsGT NP_002108.4:n.*263_*264delinsGT
NM_002117.6:c.*263_*264delinsGT MANE Select NP_002108.4:n.*263_*264delinsGT