Canonical Allele Identifier: CA2465005595

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149487077C= , CM000685.2:g.149487077C=	GRCh38
NC_000023.10:g.148568608C= , CM000685.1:g.148568608C=	GRCh37
NC_000023.9:g.148376513C=	NCBI36
NG_011900.3:g.23258G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1028G= MANE Select	ENSP00000339801.6:p.Gly343=
ENST00000651111.1:c.395G=	ENSP00000498395.1:p.Gly132=
ENST00000340855.10:c.1028G=	ENSP00000339801.6:p.Gly343=
ENST00000422081.6:c.395G=	ENSP00000477056.1:p.Gly132=
ENST00000441880.1:n.135G=
NM_000202.6:c.1028G=	NP_000193.1:p.Gly343=
NM_001166550.2:c.758G=	NP_001160022.1:p.Gly253=
NM_000202.7:c.1028G=	NP_000193.1:p.Gly343=
NM_001166550.3:c.758G=	NP_001160022.1:p.Gly253=
NM_000202.8:c.1028G= MANE Select	NP_000193.1:p.Gly343=
NM_001166550.4:c.758G=	NP_001160022.1:p.Gly253=