Canonical Allele Identifier: CA2465010057

Gene: IDS

Linked Data

• dbSNP Id: rs2089474237

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149500904_149500905del , CM000685.2:g.149500904_149500905del	GRCh38
NC_000023.10:g.148582435_148582436del , CM000685.1:g.148582435_148582436del	GRCh37
NC_000023.9:g.148390340_148390341del	NCBI36
NG_011900.3:g.9430_9431del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.507+44_507+45del MANE Select	ENSP00000339801.6:n.507+44_507+45del
ENST00000651111.1:c.-127+44_-127+45del	ENSP00000498395.1:n.-127+44_-127+45del
ENST00000340855.10:c.507+44_507+45del	ENSP00000339801.6:n.507+44_507+45del
ENST00000370441.8:c.507+44_507+45del	ENSP00000359470.4:n.507+44_507+45del
ENST00000422081.6:c.-127+44_-127+45del	ENSP00000477056.1:n.-127+44_-127+45del
ENST00000441880.1:n.114-13807_114-13806del
ENST00000464251.5:c.433+44_433+45del	ENSP00000428980.1:n.433+44_433+45del
ENST00000466323.5:c.507+44_507+45del	ENSP00000418264.1:n.507+44_507+45del
ENST00000490775.5:n.166+44_166+45del
ENST00000523759.5:n.621+44_621+45del
NM_000202.6:c.507+44_507+45del	NP_000193.1:n.507+44_507+45del
NM_001166550.2:c.237+44_237+45del	NP_001160022.1:n.237+44_237+45del
NM_006123.4:c.507+44_507+45del	NP_006114.1:n.507+44_507+45del
NR_104128.1:n.724+44_724+45del
NM_000202.7:c.507+44_507+45del	NP_000193.1:n.507+44_507+45del
NM_001166550.3:c.237+44_237+45del	NP_001160022.1:n.237+44_237+45del
NM_000202.8:c.507+44_507+45del MANE Select	NP_000193.1:n.507+44_507+45del
NM_001166550.4:c.237+44_237+45del	NP_001160022.1:n.237+44_237+45del
NM_006123.5:c.507+44_507+45del	NP_006114.1:n.507+44_507+45del
NR_104128.2:n.676+44_676+45del