Canonical Allele Identifier: CA2739289620

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149501024del , CM000685.2:g.149501024del	GRCh38
NC_000023.10:g.148582555del , CM000685.1:g.148582555del	GRCh37
NC_000023.9:g.148390460del	NCBI36
NG_011900.3:g.9312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.433del MANE Select	ENSP00000339801.6:p.His145IlefsTer?
ENST00000651111.1:c.-201del	ENSP00000498395.1:n.-201del
ENST00000340855.10:c.433del	ENSP00000339801.6:p.His145IlefsTer?
ENST00000370441.8:c.433del	ENSP00000359470.4:p.His145IlefsTer?
ENST00000422081.6:c.-201del	ENSP00000477056.1:n.-201del
ENST00000441880.1:n.114-13925del
ENST00000464251.5:c.359del	ENSP00000428980.1:n.359del
ENST00000466323.5:c.433del	ENSP00000418264.1:p.His145IlefsTer?
ENST00000490775.5:n.92del
ENST00000523759.5:n.547del
NM_000202.6:c.433del	NP_000193.1:p.His145IlefsTer?
NM_001166550.2:c.163del	NP_001160022.1:p.His55IlefsTer?
NM_006123.4:c.433del	NP_006114.1:p.His145IlefsTer?
NR_104128.1:n.650del
NM_000202.7:c.433del	NP_000193.1:p.His145IlefsTer?
NM_001166550.3:c.163del	NP_001160022.1:p.His55IlefsTer?
NM_000202.8:c.433del MANE Select	NP_000193.1:p.His145IlefsTer?
NM_001166550.4:c.163del	NP_001160022.1:p.His55IlefsTer?
NM_006123.5:c.433del	NP_006114.1:p.His145IlefsTer?
NR_104128.2:n.602del