Canonical Allele Identifier: CA2680762835
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150399065del , CM000668.2:g.150399065del GRCh38
NC_000006.11:g.150720201del , CM000668.1:g.150720201del GRCh37
NC_000006.10:g.150761894del NCBI36
NG_016007.1:g.35174del
NG_016007.2:g.35174del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*828del MANE Select ENSP00000343763.4:n.*828del
ENST00000229447.9:c.*928del ENSP00000229447.5:n.*928del
ENST00000344419.7:c.*828del ENSP00000343763.3:n.*828del
NM_001164694.1:c.*928del NP_001158166.1:n.*928del
NM_001164695.1:c.*1015del NP_001158167.1:n.*1015del
NM_203395.2:c.*828del NP_981932.1:n.*828del
NM_001318495.1:c.*828del NP_001305424.1:n.*828del
NR_134655.1:n.2011del
NM_001164694.2:c.*928del NP_001158166.1:n.*928del
NM_001164695.2:c.*1015del NP_001158167.1:n.*1015del
NM_001318495.2:c.*828del NP_001305424.1:n.*828del
NM_203395.3:c.*828del MANE Select NP_981932.1:n.*828del
NR_134655.2:n.1891del