Canonical Allele Identifier: CA2677950145
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269838del , CM000668.2:g.31269838del GRCh38
NC_000006.11:g.31237615del , CM000668.1:g.31237615del GRCh37
NC_000006.10:g.31345594del NCBI36
NG_029422.2:g.7296del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+130del MANE Select ENSP00000365402.5:n.1015+130del
ENST00000376228.9:c.1015+130del ENSP00000365402.5:n.1015+130del
ENST00000376237.8:c.*602+130del ENSP00000365412.4:n.*602+130del
ENST00000383329.7:c.1015+130del ENSP00000372819.3:n.1015+130del
ENST00000470363.5:n.463del
ENST00000487245.5:n.1374+130del
NM_002117.5:c.1015+130del NP_002108.4:n.1015+130del
NM_002117.6:c.1015+130del MANE Select NP_002108.4:n.1015+130del