Canonical Allele Identifier: CA2677949685
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269407dup , CM000668.2:g.31269407dup GRCh38
NC_000006.11:g.31237184dup , CM000668.1:g.31237184dup GRCh37
NC_000006.10:g.31345163dup NCBI36
NG_029422.2:g.7725dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-22dup MANE Select ENSP00000365402.5:n.1049-22dup
ENST00000376228.9:c.1049-22dup ENSP00000365402.5:n.1049-22dup
ENST00000376237.8:c.*636-22dup ENSP00000365412.4:n.*636-22dup
ENST00000383329.7:c.1067-22dup ENSP00000372819.3:n.1067-22dup
ENST00000466892.5:n.260dup
ENST00000470363.5:n.807-22dup
ENST00000487245.5:n.1408-22dup
NM_002117.5:c.1049-22dup NP_002108.4:n.1049-22dup
NM_002117.6:c.1049-22dup MANE Select NP_002108.4:n.1049-22dup