Canonical Allele Identifier: CA2677949850
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269594del , CM000668.2:g.31269594del GRCh38
NC_000006.11:g.31237371del , CM000668.1:g.31237371del GRCh37
NC_000006.10:g.31345350del NCBI36
NG_029422.2:g.7539del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1016-68del MANE Select ENSP00000365402.5:n.1016-68del
ENST00000376228.9:c.1016-68del ENSP00000365402.5:n.1016-68del
ENST00000376237.8:c.*603-68del ENSP00000365412.4:n.*603-68del
ENST00000383329.7:c.1016-50del ENSP00000372819.3:n.1016-50del
ENST00000466892.5:n.74del
ENST00000470363.5:n.706del
ENST00000487245.5:n.1375-68del
NM_002117.5:c.1016-68del NP_002108.4:n.1016-68del
NM_002117.6:c.1016-68del MANE Select NP_002108.4:n.1016-68del