Canonical Allele Identifier: CA2695236627

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498113del , CM000685.2:g.149498113del	GRCh38
NC_000023.10:g.148579644del , CM000685.1:g.148579644del	GRCh37
NC_000023.9:g.148387549del	NCBI36
NG_011900.3:g.12225del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.705del MANE Select	ENSP00000339801.6:p.Lys236ArgfsTer?
ENST00000651111.1:c.72del	ENSP00000498395.1:p.Lys25ArgfsTer?
ENST00000340855.10:c.705del	ENSP00000339801.6:p.Lys236ArgfsTer?
ENST00000370441.8:c.705del	ENSP00000359470.4:p.Lys236ArgfsTer?
ENST00000422081.6:c.72del	ENSP00000477056.1:p.Lys25ArgfsTer?
ENST00000441880.1:n.114-11012del
ENST00000464251.5:c.631del	ENSP00000428980.1:n.631del
ENST00000466019.1:n.157del
ENST00000466323.5:c.705del	ENSP00000418264.1:p.Lys236ArgfsTer?
ENST00000490775.5:n.490del
NM_000202.6:c.705del	NP_000193.1:p.Lys236ArgfsTer?
NM_001166550.2:c.435del	NP_001160022.1:p.Lys146ArgfsTer?
NM_006123.4:c.705del	NP_006114.1:p.Lys236ArgfsTer?
NR_104128.1:n.922del
NM_000202.7:c.705del	NP_000193.1:p.Lys236ArgfsTer?
NM_001166550.3:c.435del	NP_001160022.1:p.Lys146ArgfsTer?
NM_000202.8:c.705del MANE Select	NP_000193.1:p.Lys236ArgfsTer?
NM_001166550.4:c.435del	NP_001160022.1:p.Lys146ArgfsTer?
NM_006123.5:c.705del	NP_006114.1:p.Lys236ArgfsTer?
NR_104128.2:n.874del