Canonical Allele Identifier: CA1619077182
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268941_31268943delinsCCA , CM000668.2:g.31268941_31268943delinsCCA GRCh38
NC_000006.11:g.31236718_31236720delinsCCA , CM000668.1:g.31236718_31236720delinsCCA GRCh37
NC_000006.10:g.31344697_31344699delinsCCA NCBI36
NG_029422.2:g.8189_8191delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*226_*228delinsTGG MANE Select ENSP00000365402.5:n.*226_*228delinsTGG
ENST00000376228.9:c.*226_*228delinsTGG ENSP00000365402.5:n.*226_*228delinsTGG
ENST00000376237.8:c.*914_*916delinsTGG ENSP00000365412.4:n.*914_*916delinsTGG
ENST00000383329.7:c.*226_*228delinsTGG ENSP00000372819.3:n.*226_*228delinsTGG
ENST00000466892.5:n.560_562delinsTGG
ENST00000470363.5:n.1085_1087delinsTGG
ENST00000487245.5:n.1686_1688delinsTGG
NM_002117.5:c.*226_*228delinsTGG NP_002108.4:n.*226_*228delinsTGG
NM_002117.6:c.*226_*228delinsTGG MANE Select NP_002108.4:n.*226_*228delinsTGG