Canonical Allele Identifier: CA2695236480

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482837del , CM000685.2:g.149482837del	GRCh38
NC_000023.10:g.148564368del , CM000685.1:g.148564368del	GRCh37
NC_000023.9:g.148372273del	NCBI36
NG_011900.3:g.27499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1563del MANE Select	ENSP00000339801.6:p.Glu521AspfsTer28
ENST00000651111.1:c.930del	ENSP00000498395.1:p.Glu310AspfsTer28
ENST00000340855.10:c.1563del	ENSP00000339801.6:p.Glu521AspfsTer28
ENST00000422081.6:c.930del	ENSP00000477056.1:p.Glu310AspfsTer28
NM_000202.6:c.1563del	NP_000193.1:p.Glu521AspfsTer28
NM_001166550.2:c.1293del	NP_001160022.1:p.Glu431AspfsTer28
NM_000202.7:c.1563del	NP_000193.1:p.Glu521AspfsTer28
NM_001166550.3:c.1293del	NP_001160022.1:p.Glu431AspfsTer28
NM_000202.8:c.1563del MANE Select	NP_000193.1:p.Glu521AspfsTer28
NM_001166550.4:c.1293del	NP_001160022.1:p.Glu431AspfsTer28