Canonical Allele Identifier: CA2524102683

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490449_149490450insA , CM000685.2:g.149490449_149490450insA	GRCh38
NC_000023.10:g.148571980_148571981insA , CM000685.1:g.148571980_148571981insA	GRCh37
NC_000023.9:g.148379885_148379886insA	NCBI36
NG_011900.3:g.19885_19886insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-10_880-9insT MANE Select	ENSP00000339801.6:n.880-10_880-9insT
ENST00000651111.1:c.247-10_247-9insT	ENSP00000498395.1:n.247-10_247-9insT
ENST00000340855.10:c.880-10_880-9insT	ENSP00000339801.6:n.880-10_880-9insT
ENST00000370441.8:c.880-10_880-9insT	ENSP00000359470.4:n.880-10_880-9insT
ENST00000422081.6:c.247-10_247-9insT	ENSP00000477056.1:n.247-10_247-9insT
ENST00000441880.1:n.114-3352_114-3351insT
ENST00000464251.5:c.806-10_806-9insT	ENSP00000428980.1:n.806-10_806-9insT
ENST00000466323.5:c.*71-10_*71-9insT	ENSP00000418264.1:n.*71-10_*71-9insT
ENST00000490775.5:n.665-10_665-9insT
NM_000202.6:c.880-10_880-9insT	NP_000193.1:n.880-10_880-9insT
NM_001166550.2:c.610-10_610-9insT	NP_001160022.1:n.610-10_610-9insT
NM_006123.4:c.880-10_880-9insT	NP_006114.1:n.880-10_880-9insT
NR_104128.1:n.1227-10_1227-9insT
NM_000202.7:c.880-10_880-9insT	NP_000193.1:n.880-10_880-9insT
NM_001166550.3:c.610-10_610-9insT	NP_001160022.1:n.610-10_610-9insT
NM_000202.8:c.880-10_880-9insT MANE Select	NP_000193.1:n.880-10_880-9insT
NM_001166550.4:c.610-10_610-9insT	NP_001160022.1:n.610-10_610-9insT
NM_006123.5:c.880-10_880-9insT	NP_006114.1:n.880-10_880-9insT
NR_104128.2:n.1179-10_1179-9insT