Canonical Allele Identifier: CA2579719145

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487142_149487144del , CM000685.2:g.149487142_149487144del	GRCh38
NC_000023.10:g.148568673_148568675del , CM000685.1:g.148568673_148568675del	GRCh37
NC_000023.9:g.148376578_148376580del	NCBI36
NG_011900.3:g.23196_23198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1007-41_1007-39del MANE Select	ENSP00000339801.6:n.1007-41_1007-39del
ENST00000651111.1:c.374-41_374-39del	ENSP00000498395.1:n.374-41_374-39del
ENST00000340855.10:c.1007-41_1007-39del	ENSP00000339801.6:n.1007-41_1007-39del
ENST00000370441.8:c.*149_*151del	ENSP00000359470.4:n.*149_*151del
ENST00000422081.6:c.374-41_374-39del	ENSP00000477056.1:n.374-41_374-39del
ENST00000441880.1:n.114-41_114-39del
ENST00000466323.5:c.*372_*374del	ENSP00000418264.1:n.*372_*374del
NM_000202.6:c.1007-41_1007-39del	NP_000193.1:n.1007-41_1007-39del
NM_001166550.2:c.737-41_737-39del	NP_001160022.1:n.737-41_737-39del
NM_006123.4:c.*149_*151del	NP_006114.1:n.*149_*151del
NR_104128.1:n.1528_1530del
NM_000202.7:c.1007-41_1007-39del	NP_000193.1:n.1007-41_1007-39del
NM_001166550.3:c.737-41_737-39del	NP_001160022.1:n.737-41_737-39del
NM_000202.8:c.1007-41_1007-39del MANE Select	NP_000193.1:n.1007-41_1007-39del
NM_001166550.4:c.737-41_737-39del	NP_001160022.1:n.737-41_737-39del
NM_006123.5:c.*149_*151del	NP_006114.1:n.*149_*151del
NR_104128.2:n.1480_1482del