Canonical Allele Identifier: CA2773539403
Gene: IYD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398791del , CM000668.2:g.150398791del GRCh38
NC_000006.11:g.150719927del , CM000668.1:g.150719927del GRCh37
NC_000006.10:g.150761620del NCBI36
NG_016007.1:g.34900del
NG_016007.2:g.34900del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*554del MANE Select ENSP00000343763.4:n.*554del
ENST00000229447.9:c.*654del ENSP00000229447.5:n.*654del
ENST00000344419.7:c.*554del ENSP00000343763.3:n.*554del
NM_001164694.1:c.*654del NP_001158166.1:n.*654del
NM_001164695.1:c.*741del NP_001158167.1:n.*741del
NM_203395.2:c.*554del NP_981932.1:n.*554del
NM_001318495.1:c.*554del NP_001305424.1:n.*554del
NR_134655.1:n.1737del
NM_001164694.2:c.*654del NP_001158166.1:n.*654del
NM_001164695.2:c.*741del NP_001158167.1:n.*741del
NM_001318495.2:c.*554del NP_001305424.1:n.*554del
NM_203395.3:c.*554del MANE Select NP_981932.1:n.*554del
NR_134655.2:n.1617del