Canonical Allele Identifier: CA2512364409

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486721_149486722insA , CM000685.2:g.149486721_149486722insA	GRCh38
NC_000023.10:g.148568252_148568253insA , CM000685.1:g.148568252_148568253insA	GRCh37
NC_000023.9:g.148376157_148376158insA	NCBI36
NG_011900.3:g.23613_23614insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1180+203_1180+204insT MANE Select	ENSP00000339801.6:n.1180+203_1180+204insT
ENST00000651111.1:c.547+203_547+204insT	ENSP00000498395.1:n.547+203_547+204insT
ENST00000340855.10:c.1180+203_1180+204insT	ENSP00000339801.6:n.1180+203_1180+204insT
ENST00000422081.6:c.547+203_547+204insT	ENSP00000477056.1:n.547+203_547+204insT
ENST00000441880.1:n.287+203_287+204insT
NM_000202.6:c.1180+203_1180+204insT	NP_000193.1:n.1180+203_1180+204insT
NM_001166550.2:c.910+203_910+204insT	NP_001160022.1:n.910+203_910+204insT
NM_000202.7:c.1180+203_1180+204insT	NP_000193.1:n.1180+203_1180+204insT
NM_001166550.3:c.910+203_910+204insT	NP_001160022.1:n.910+203_910+204insT
NM_000202.8:c.1180+203_1180+204insT MANE Select	NP_000193.1:n.1180+203_1180+204insT
NM_001166550.4:c.910+203_910+204insT	NP_001160022.1:n.910+203_910+204insT