Canonical Allele Identifier: CA1087448885
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268906_31268907insA , CM000668.2:g.31268906_31268907insA GRCh38
NC_000006.11:g.31236683_31236684insA , CM000668.1:g.31236683_31236684insA GRCh37
NC_000006.10:g.31344662_31344663insA NCBI36
NG_029422.2:g.8225_8226insT

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*262_*263insT MANE Select ENSP00000365402.5:n.*262_*263insT
ENST00000376228.9:c.*262_*263insT ENSP00000365402.5:n.*262_*263insT
ENST00000376237.8:c.*950_*951insT ENSP00000365412.4:n.*950_*951insT
ENST00000383329.7:c.*262_*263insT ENSP00000372819.3:n.*262_*263insT
ENST00000466892.5:n.596_597insT
ENST00000470363.5:n.1121_1122insT
ENST00000487245.5:n.1722_1723insT
NM_002117.5:c.*262_*263insT NP_002108.4:n.*262_*263insT
NM_002117.6:c.*262_*263insT MANE Select NP_002108.4:n.*262_*263insT