Canonical Allele Identifier: CA2465004048

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483102T= , CM000685.2:g.149483102T=	GRCh38
NC_000023.10:g.148564633T= , CM000685.1:g.148564633T=	GRCh37
NC_000023.9:g.148372538T=	NCBI36
NG_011900.3:g.27233A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1297A= MANE Select	ENSP00000339801.6:p.Arg433=
ENST00000651111.1:c.664A=	ENSP00000498395.1:p.Arg222=
ENST00000340855.10:c.1297A=	ENSP00000339801.6:p.Arg433=
ENST00000422081.6:c.664A=	ENSP00000477056.1:p.Arg222=
ENST00000441880.1:n.404A=
NM_000202.6:c.1297A=	NP_000193.1:p.Arg433=
NM_001166550.2:c.1027A=	NP_001160022.1:p.Arg343=
NM_000202.7:c.1297A=	NP_000193.1:p.Arg433=
NM_001166550.3:c.1027A=	NP_001160022.1:p.Arg343=
NM_000202.8:c.1297A= MANE Select	NP_000193.1:p.Arg433=
NM_001166550.4:c.1027A=	NP_001160022.1:p.Arg343=