Canonical Allele Identifier: CA2550093332

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486707_149486718del , CM000685.2:g.149486707_149486718del	GRCh38
NC_000023.10:g.148568238_148568249del , CM000685.1:g.148568238_148568249del	GRCh37
NC_000023.9:g.148376143_148376154del	NCBI36
NG_011900.3:g.23617_23628del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1180+207_1180+218del MANE Select	ENSP00000339801.6:n.1180+207_1180+218del
ENST00000651111.1:c.547+207_547+218del	ENSP00000498395.1:n.547+207_547+218del
ENST00000340855.10:c.1180+207_1180+218del	ENSP00000339801.6:n.1180+207_1180+218del
ENST00000422081.6:c.547+207_547+218del	ENSP00000477056.1:n.547+207_547+218del
ENST00000441880.1:n.287+207_287+218del
NM_000202.6:c.1180+207_1180+218del	NP_000193.1:n.1180+207_1180+218del
NM_001166550.2:c.910+207_910+218del	NP_001160022.1:n.910+207_910+218del
NM_000202.7:c.1180+207_1180+218del	NP_000193.1:n.1180+207_1180+218del
NM_001166550.3:c.910+207_910+218del	NP_001160022.1:n.910+207_910+218del
NM_000202.8:c.1180+207_1180+218del MANE Select	NP_000193.1:n.1180+207_1180+218del
NM_001166550.4:c.910+207_910+218del	NP_001160022.1:n.910+207_910+218del