Canonical Allele Identifier: CA519059552

Gene: IDS

Linked Data

• dbSNP Id: rs1141608
• gnomAD v4: X-149501018-G-T
• MyVariant Identifiers: chrX:g.148582549G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149501018G>T , CM000685.2:g.149501018G>T	GRCh38
NC_000023.10:g.148582549G>T , CM000685.1:g.148582549G>T	GRCh37
NC_000023.9:g.148390454G>T	NCBI36
NG_011900.3:g.9317C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.438C>A MANE Select	ENSP00000339801.6:p.Thr146=
ENST00000651111.1:c.-196C>A	ENSP00000498395.1:n.-196C>A
ENST00000340855.10:c.438C>A	ENSP00000339801.6:p.Thr146=
ENST00000370441.8:c.438C>A	ENSP00000359470.4:p.Thr146=
ENST00000422081.6:c.-196C>A	ENSP00000477056.1:n.-196C>A
ENST00000441880.1:n.114-13920C>A
ENST00000464251.5:c.364C>A	ENSP00000428980.1:n.364C>A
ENST00000466323.5:c.438C>A	ENSP00000418264.1:p.Thr146=
ENST00000490775.5:n.97C>A
ENST00000523759.5:n.552C>A
NM_000202.6:c.438C>A	NP_000193.1:p.Thr146=
NM_001166550.2:c.168C>A	NP_001160022.1:p.Thr56=
NM_006123.4:c.438C>A	NP_006114.1:p.Thr146=
NR_104128.1:n.655C>A
NM_000202.7:c.438C>A	NP_000193.1:p.Thr146=
NM_001166550.3:c.168C>A	NP_001160022.1:p.Thr56=
NM_000202.8:c.438C>A MANE Select	NP_000193.1:p.Thr146=
NM_001166550.4:c.168C>A	NP_001160022.1:p.Thr56=
NM_006123.5:c.438C>A	NP_006114.1:p.Thr146=
NR_104128.2:n.607C>A