Canonical Allele Identifier: CA2680762672
Gene: IYD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.150398946_150398947del , CM000668.2:g.150398946_150398947del GRCh38
NC_000006.11:g.150720082_150720083del , CM000668.1:g.150720082_150720083del GRCh37
NC_000006.10:g.150761775_150761776del NCBI36
NG_016007.1:g.35055_35056del
NG_016007.2:g.35055_35056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000344419.8:c.*709_*710del MANE Select ENSP00000343763.4:n.*709_*710del
ENST00000229447.9:c.*809_*810del ENSP00000229447.5:n.*809_*810del
ENST00000344419.7:c.*709_*710del ENSP00000343763.3:n.*709_*710del
NM_001164694.1:c.*809_*810del NP_001158166.1:n.*809_*810del
NM_001164695.1:c.*896_*897del NP_001158167.1:n.*896_*897del
NM_203395.2:c.*709_*710del NP_981932.1:n.*709_*710del
NM_001318495.1:c.*709_*710del NP_001305424.1:n.*709_*710del
NR_134655.1:n.1892_1893del
NM_001164694.2:c.*809_*810del NP_001158166.1:n.*809_*810del
NM_001164695.2:c.*896_*897del NP_001158167.1:n.*896_*897del
NM_001318495.2:c.*709_*710del NP_001305424.1:n.*709_*710del
NM_203395.3:c.*709_*710del MANE Select NP_981932.1:n.*709_*710del
NR_134655.2:n.1772_1773del