Canonical Allele Identifier: CA2538080060
Gene: IDS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.149490828_149490830del , CM000685.2:g.149490828_149490830del GRCh38
NC_000023.10:g.148572359_148572361del , CM000685.1:g.148572359_148572361del GRCh37
NC_000023.9:g.148380264_148380266del NCBI36
NG_011900.3:g.19509_19511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340855.11:c.880-386_880-384del MANE Select ENSP00000339801.6:n.880-386_880-384del
ENST00000651111.1:c.247-386_247-384del ENSP00000498395.1:n.247-386_247-384del
ENST00000340855.10:c.880-386_880-384del ENSP00000339801.6:n.880-386_880-384del
ENST00000370441.8:c.880-386_880-384del ENSP00000359470.4:n.880-386_880-384del
ENST00000422081.6:c.247-386_247-384del ENSP00000477056.1:n.247-386_247-384del
ENST00000441880.1:n.114-3728_114-3726del
ENST00000464251.5:c.806-386_806-384del ENSP00000428980.1:n.806-386_806-384del
ENST00000466323.5:c.*71-386_*71-384del ENSP00000418264.1:n.*71-386_*71-384del
ENST00000490775.5:n.665-386_665-384del
NM_000202.6:c.880-386_880-384del NP_000193.1:n.880-386_880-384del
NM_001166550.2:c.610-386_610-384del NP_001160022.1:n.610-386_610-384del
NM_006123.4:c.880-386_880-384del NP_006114.1:n.880-386_880-384del
NR_104128.1:n.1227-386_1227-384del
NM_000202.7:c.880-386_880-384del NP_000193.1:n.880-386_880-384del
NM_001166550.3:c.610-386_610-384del NP_001160022.1:n.610-386_610-384del
NM_000202.8:c.880-386_880-384del MANE Select NP_000193.1:n.880-386_880-384del
NM_001166550.4:c.610-386_610-384del NP_001160022.1:n.610-386_610-384del
NM_006123.5:c.880-386_880-384del NP_006114.1:n.880-386_880-384del
NR_104128.2:n.1179-386_1179-384del