Canonical Allele Identifier: CA2695236561

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149500999del , CM000685.2:g.149500999del	GRCh38
NC_000023.10:g.148582530del , CM000685.1:g.148582530del	GRCh37
NC_000023.9:g.148390435del	NCBI36
NG_011900.3:g.9336del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.457del MANE Select	ENSP00000339801.6:p.Trp153GlyfsTer?
ENST00000651111.1:c.-177del	ENSP00000498395.1:n.-177del
ENST00000340855.10:c.457del	ENSP00000339801.6:p.Trp153GlyfsTer?
ENST00000370441.8:c.457del	ENSP00000359470.4:p.Trp153GlyfsTer?
ENST00000422081.6:c.-177del	ENSP00000477056.1:n.-177del
ENST00000441880.1:n.114-13901del
ENST00000464251.5:c.383del	ENSP00000428980.1:n.383del
ENST00000466323.5:c.457del	ENSP00000418264.1:p.Trp153GlyfsTer?
ENST00000490775.5:n.116del
ENST00000523759.5:n.571del
NM_000202.6:c.457del	NP_000193.1:p.Trp153GlyfsTer?
NM_001166550.2:c.187del	NP_001160022.1:p.Trp63GlyfsTer?
NM_006123.4:c.457del	NP_006114.1:p.Trp153GlyfsTer?
NR_104128.1:n.674del
NM_000202.7:c.457del	NP_000193.1:p.Trp153GlyfsTer?
NM_001166550.3:c.187del	NP_001160022.1:p.Trp63GlyfsTer?
NM_000202.8:c.457del MANE Select	NP_000193.1:p.Trp153GlyfsTer?
NM_001166550.4:c.187del	NP_001160022.1:p.Trp63GlyfsTer?
NM_006123.5:c.457del	NP_006114.1:p.Trp153GlyfsTer?
NR_104128.2:n.626del