Canonical Allele Identifier: CA2677949710
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269422del , CM000668.2:g.31269422del GRCh38
NC_000006.11:g.31237199del , CM000668.1:g.31237199del GRCh37
NC_000006.10:g.31345178del NCBI36
NG_029422.2:g.7712del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-35del MANE Select ENSP00000365402.5:n.1049-35del
ENST00000376228.9:c.1049-35del ENSP00000365402.5:n.1049-35del
ENST00000376237.8:c.*636-35del ENSP00000365412.4:n.*636-35del
ENST00000383329.7:c.1067-35del ENSP00000372819.3:n.1067-35del
ENST00000466892.5:n.247del
ENST00000470363.5:n.807-35del
ENST00000487245.5:n.1408-35del
NM_002117.5:c.1049-35del NP_002108.4:n.1049-35del
NM_002117.6:c.1049-35del MANE Select NP_002108.4:n.1049-35del