Canonical Allele Identifier: CA2695236596

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503415dup , CM000685.2:g.149503415dup	GRCh38
NC_000023.10:g.148584945dup , CM000685.1:g.148584945dup	GRCh37
NC_000023.9:g.148392850dup	NCBI36
NG_011900.3:g.6920dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.315dup MANE Select	ENSP00000339801.6:p.Asn106GlnfsTer?
ENST00000651111.1:c.-215-2378dup	ENSP00000498395.1:n.-215-2378dup
ENST00000340855.10:c.315dup	ENSP00000339801.6:p.Asn106GlnfsTer?
ENST00000370441.8:c.315dup	ENSP00000359470.4:p.Asn106GlnfsTer?
ENST00000422081.6:c.-215-2378dup	ENSP00000477056.1:n.-215-2378dup
ENST00000427113.2:n.770-1192dup
ENST00000428056.6:c.315dup	ENSP00000390241.2:p.Asn106GlnfsTer?
ENST00000441880.1:n.114-16317dup
ENST00000464251.5:c.138dup	ENSP00000428980.1:p.Asn47GlnfsTer?
ENST00000466323.5:c.315dup	ENSP00000418264.1:p.Asn106GlnfsTer?
ENST00000523759.5:n.533-2378dup
NM_000202.6:c.315dup	NP_000193.1:p.Asn106GlnfsTer?
NM_001166550.2:c.45dup	NP_001160022.1:p.Asn16GlnfsTer?
NM_006123.4:c.315dup	NP_006114.1:p.Asn106GlnfsTer?
NR_104128.1:n.532dup
NM_000202.7:c.315dup	NP_000193.1:p.Asn106GlnfsTer?
NM_001166550.3:c.45dup	NP_001160022.1:p.Asn16GlnfsTer?
NM_000202.8:c.315dup MANE Select	NP_000193.1:p.Asn106GlnfsTer?
NM_001166550.4:c.45dup	NP_001160022.1:p.Asn16GlnfsTer?
NM_006123.5:c.315dup	NP_006114.1:p.Asn106GlnfsTer?
NR_104128.2:n.484dup