Canonical Allele Identifier: CA2465005497

Gene: IDS

Linked Data

• dbSNP Id: rs2089339656

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486825_149486826insA , CM000685.2:g.149486825_149486826insA	GRCh38
NC_000023.10:g.148568356_148568357insA , CM000685.1:g.148568356_148568357insA	GRCh37
NC_000023.9:g.148376261_148376262insA	NCBI36
NG_011900.3:g.23509_23510insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1180+99_1180+100insT MANE Select	ENSP00000339801.6:n.1180+99_1180+100insT
ENST00000651111.1:c.547+99_547+100insT	ENSP00000498395.1:n.547+99_547+100insT
ENST00000340855.10:c.1180+99_1180+100insT	ENSP00000339801.6:n.1180+99_1180+100insT
ENST00000422081.6:c.547+99_547+100insT	ENSP00000477056.1:n.547+99_547+100insT
ENST00000441880.1:n.287+99_287+100insT
NM_000202.6:c.1180+99_1180+100insT	NP_000193.1:n.1180+99_1180+100insT
NM_001166550.2:c.910+99_910+100insT	NP_001160022.1:n.910+99_910+100insT
NM_000202.7:c.1180+99_1180+100insT	NP_000193.1:n.1180+99_1180+100insT
NM_001166550.3:c.910+99_910+100insT	NP_001160022.1:n.910+99_910+100insT
NM_000202.8:c.1180+99_1180+100insT MANE Select	NP_000193.1:n.1180+99_1180+100insT
NM_001166550.4:c.910+99_910+100insT	NP_001160022.1:n.910+99_910+100insT