Canonical Allele Identifier: CA519058373

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579752G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498221G>A , CM000685.2:g.149498221G>A	GRCh38
NC_000023.10:g.148579752G>A , CM000685.1:g.148579752G>A	GRCh37
NC_000023.9:g.148387657G>A	NCBI36
NG_011900.3:g.12114C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.594C>T MANE Select	ENSP00000339801.6:p.Asp198=
ENST00000651111.1:c.-40C>T	ENSP00000498395.1:n.-40C>T
ENST00000340855.10:c.594C>T	ENSP00000339801.6:p.Asp198=
ENST00000370441.8:c.594C>T	ENSP00000359470.4:p.Asp198=
ENST00000422081.6:c.-40C>T	ENSP00000477056.1:n.-40C>T
ENST00000441880.1:n.114-11123C>T
ENST00000464251.5:c.520C>T	ENSP00000428980.1:n.520C>T
ENST00000466019.1:n.46C>T
ENST00000466323.5:c.594C>T	ENSP00000418264.1:p.Asp198=
ENST00000490775.5:n.379C>T
ENST00000523759.5:n.708C>T
NM_000202.6:c.594C>T	NP_000193.1:p.Asp198=
NM_001166550.2:c.324C>T	NP_001160022.1:p.Asp108=
NM_006123.4:c.594C>T	NP_006114.1:p.Asp198=
NR_104128.1:n.811C>T
NM_000202.7:c.594C>T	NP_000193.1:p.Asp198=
NM_001166550.3:c.324C>T	NP_001160022.1:p.Asp108=
NM_000202.8:c.594C>T MANE Select	NP_000193.1:p.Asp198=
NM_001166550.4:c.324C>T	NP_001160022.1:p.Asp108=
NM_006123.5:c.594C>T	NP_006114.1:p.Asp198=
NR_104128.2:n.763C>T