Canonical Allele Identifier: CA2680762919
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399132del , CM000668.2:g.150399132del GRCh38
NC_000006.11:g.150720268del , CM000668.1:g.150720268del GRCh37
NC_000006.10:g.150761961del NCBI36
NG_016007.1:g.35241del
NG_016007.2:g.35241del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*895del MANE Select ENSP00000343763.4:n.*895del
ENST00000229447.9:c.*995del ENSP00000229447.5:n.*995del
ENST00000344419.7:c.*895del ENSP00000343763.3:n.*895del
NM_001164694.1:c.*995del NP_001158166.1:n.*995del
NM_001164695.1:c.*1082del NP_001158167.1:n.*1082del
NM_203395.2:c.*895del NP_981932.1:n.*895del
NM_001318495.1:c.*895del NP_001305424.1:n.*895del
NR_134655.1:n.2078del
NM_001164694.2:c.*995del NP_001158166.1:n.*995del
NM_001164695.2:c.*1082del NP_001158167.1:n.*1082del
NM_001318495.2:c.*895del NP_001305424.1:n.*895del
NM_203395.3:c.*895del MANE Select NP_981932.1:n.*895del
NR_134655.2:n.1958del