Canonical Allele Identifier: CA2465010887

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503437T= , CM000685.2:g.149503437T=	GRCh38
NC_000023.10:g.148584967T= , CM000685.1:g.148584967T=	GRCh37
NC_000023.9:g.148392872T=	NCBI36
NG_011900.3:g.6898A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.293A= MANE Select	ENSP00000339801.6:p.Asp98=
ENST00000651111.1:c.-215-2400A=	ENSP00000498395.1:n.-215-2400A=
ENST00000340855.10:c.293A=	ENSP00000339801.6:p.Asp98=
ENST00000370441.8:c.293A=	ENSP00000359470.4:p.Asp98=
ENST00000422081.6:c.-215-2400A=	ENSP00000477056.1:n.-215-2400A=
ENST00000427113.2:n.770-1214A=
ENST00000428056.6:c.293A=	ENSP00000390241.2:p.Asp98=
ENST00000441880.1:n.114-16339A=
ENST00000464251.5:c.116A=	ENSP00000428980.1:p.Asp39=
ENST00000466323.5:c.293A=	ENSP00000418264.1:p.Asp98=
ENST00000523759.5:n.533-2400A=
NM_000202.6:c.293A=	NP_000193.1:p.Asp98=
NM_001166550.2:c.23A=	NP_001160022.1:p.Asp8=
NM_006123.4:c.293A=	NP_006114.1:p.Asp98=
NR_104128.1:n.510A=
NM_000202.7:c.293A=	NP_000193.1:p.Asp98=
NM_001166550.3:c.23A=	NP_001160022.1:p.Asp8=
NM_000202.8:c.293A= MANE Select	NP_000193.1:p.Asp98=
NM_001166550.4:c.23A=	NP_001160022.1:p.Asp8=
NM_006123.5:c.293A=	NP_006114.1:p.Asp98=
NR_104128.2:n.462A=