Canonical Allele Identifier: CA2465011150

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149504208A= , CM000685.2:g.149504208A=	GRCh38
NC_000023.10:g.148585738A= , CM000685.1:g.148585738A=	GRCh37
NC_000023.9:g.148393642A=	NCBI36
NG_011900.3:g.6127T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.189T= MANE Select	ENSP00000339801.6:p.Asn63=
ENST00000651111.1:c.-215-3171T=	ENSP00000498395.1:n.-215-3171T=
ENST00000340855.10:c.189T=	ENSP00000339801.6:p.Asn63=
ENST00000370441.8:c.189T=	ENSP00000359470.4:p.Asn63=
ENST00000422081.6:c.-215-3171T=	ENSP00000477056.1:n.-215-3171T=
ENST00000427113.2:n.770-1985T=
ENST00000428056.6:c.189T=	ENSP00000390241.2:p.Asn63=
ENST00000441880.1:n.114-17110T=
ENST00000464251.5:c.12T=	ENSP00000428980.1:p.Asn4=
ENST00000466323.5:c.189T=	ENSP00000418264.1:p.Asn63=
ENST00000521702.1:c.189T=	ENSP00000429745.1:p.Asn63=
ENST00000523759.5:n.533-3171T=
NM_000202.6:c.189T=	NP_000193.1:p.Asn63=
NM_001166550.2:c.-38T=	NP_001160022.1:n.-38T=
NM_006123.4:c.189T=	NP_006114.1:p.Asn63=
NR_104128.1:n.406T=
NM_000202.7:c.189T=	NP_000193.1:p.Asn63=
NM_001166550.3:c.-38T=	NP_001160022.1:n.-38T=
NM_000202.8:c.189T= MANE Select	NP_000193.1:p.Asn63=
NM_001166550.4:c.-38T=	NP_001160022.1:n.-38T=
NM_006123.5:c.189T=	NP_006114.1:p.Asn63=
NR_104128.2:n.358T=