Canonical Allele Identifier: CA1619078409
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761148732

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269798_31269799del , CM000668.2:g.31269798_31269799del GRCh38
NC_000006.11:g.31237575_31237576del , CM000668.1:g.31237575_31237576del GRCh37
NC_000006.10:g.31345554_31345555del NCBI36
NG_029422.2:g.7333_7334del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+167_1015+168del MANE Select ENSP00000365402.5:n.1015+167_1015+168del
ENST00000376228.9:c.1015+167_1015+168del ENSP00000365402.5:n.1015+167_1015+168del
ENST00000376237.8:c.*602+167_*602+168del ENSP00000365412.4:n.*602+167_*602+168del
ENST00000383329.7:c.1015+167_1015+168del ENSP00000372819.3:n.1015+167_1015+168del
ENST00000470363.5:n.500_501del
ENST00000487245.5:n.1374+167_1374+168del
NM_002117.5:c.1015+167_1015+168del NP_002108.4:n.1015+167_1015+168del
NM_002117.6:c.1015+167_1015+168del MANE Select NP_002108.4:n.1015+167_1015+168del