Canonical Allele Identifier: CA2677950051
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269757del , CM000668.2:g.31269757del GRCh38
NC_000006.11:g.31237534del , CM000668.1:g.31237534del GRCh37
NC_000006.10:g.31345513del NCBI36
NG_029422.2:g.7378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+212del MANE Select ENSP00000365402.5:n.1015+212del
ENST00000376228.9:c.1015+212del ENSP00000365402.5:n.1015+212del
ENST00000376237.8:c.*602+212del ENSP00000365412.4:n.*602+212del
ENST00000383329.7:c.1016-211del ENSP00000372819.3:n.1016-211del
ENST00000470363.5:n.545del
ENST00000487245.5:n.1374+212del
NM_002117.5:c.1015+212del NP_002108.4:n.1015+212del
NM_002117.6:c.1015+212del MANE Select NP_002108.4:n.1015+212del