Canonical Allele Identifier: CA2677949321
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269063dup , CM000668.2:g.31269063dup GRCh38
NC_000006.11:g.31236840dup , CM000668.1:g.31236840dup GRCh37
NC_000006.10:g.31344819dup NCBI36
NG_029422.2:g.8069dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*106dup MANE Select ENSP00000365402.5:n.*106dup
ENST00000376228.9:c.*106dup ENSP00000365402.5:n.*106dup
ENST00000376237.8:c.*794dup ENSP00000365412.4:n.*794dup
ENST00000383329.7:c.*106dup ENSP00000372819.3:n.*106dup
ENST00000466892.5:n.440dup
ENST00000470363.5:n.965dup
ENST00000487245.5:n.1566dup
NM_002117.5:c.*106dup NP_002108.4:n.*106dup
NM_002117.6:c.*106dup MANE Select NP_002108.4:n.*106dup