Canonical Allele Identifier: CA2677950616
Gene: HLA-C HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270183_31270186del , CM000668.2:g.31270183_31270186del GRCh38
NC_000006.11:g.31237960_31237963del , CM000668.1:g.31237960_31237963del GRCh37
NC_000006.10:g.31345939_31345942del NCBI36
NG_029422.2:g.6946_6949del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+24_895+27del MANE Select ENSP00000365402.5:n.895+24_895+27del
ENST00000376228.9:c.895+24_895+27del ENSP00000365402.5:n.895+24_895+27del
ENST00000376237.8:c.*482+24_*482+27del ENSP00000365412.4:n.*482+24_*482+27del
ENST00000383329.7:c.895+24_895+27del ENSP00000372819.3:n.895+24_895+27del
ENST00000470363.5:n.213+24_213+27del
ENST00000487245.5:n.1254+24_1254+27del
NM_002117.5:c.895+24_895+27del NP_002108.4:n.895+24_895+27del
NM_002117.6:c.895+24_895+27del MANE Select NP_002108.4:n.895+24_895+27del