Canonical Allele Identifier: CA2677949673
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269404_31269406dup , CM000668.2:g.31269404_31269406dup GRCh38
NC_000006.11:g.31237181_31237183dup , CM000668.1:g.31237181_31237183dup GRCh37
NC_000006.10:g.31345160_31345162dup NCBI36
NG_029422.2:g.7732_7734dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-15_1049-13dup MANE Select ENSP00000365402.5:n.1049-15_1049-13dup
ENST00000376228.9:c.1049-15_1049-13dup ENSP00000365402.5:n.1049-15_1049-13dup
ENST00000376237.8:c.*636-15_*636-13dup ENSP00000365412.4:n.*636-15_*636-13dup
ENST00000383329.7:c.1067-15_1067-13dup ENSP00000372819.3:n.1067-15_1067-13dup
ENST00000466892.5:n.267_269dup
ENST00000470363.5:n.807-15_807-13dup
ENST00000487245.5:n.1408-15_1408-13dup
NM_002117.5:c.1049-15_1049-13dup NP_002108.4:n.1049-15_1049-13dup
NM_002117.6:c.1049-15_1049-13dup MANE Select NP_002108.4:n.1049-15_1049-13dup