Canonical Allele Identifier: CA10537535

Gene: IDS

Linked Data

• ClinVar Variation Id: 2041011
• ClinVar RCV Id: RCV002912825
• dbSNP Id: rs782704207
• ExAC: X:148571856 G / A
• gnomAD v2: X-148571856-G-A
• gnomAD v3: X-149490325-G-A
• gnomAD v4: X-149490325-G-A
• MyVariant Identifiers: chrX:g.148571856G>A (hg19) ; chrX:g.149490325G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490325G>A , CM000685.2:g.149490325G>A	GRCh38
NC_000023.10:g.148571856G>A , CM000685.1:g.148571856G>A	GRCh37
NC_000023.9:g.148379761G>A	NCBI36
NG_011900.3:g.20010C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.995C>T MANE Select	ENSP00000339801.6:p.Thr332Ile
ENST00000651111.1:c.362C>T	ENSP00000498395.1:p.Thr121Ile
ENST00000340855.10:c.995C>T	ENSP00000339801.6:p.Thr332Ile
ENST00000370441.8:c.995C>T	ENSP00000359470.4:p.Thr332Ile
ENST00000422081.6:c.362C>T	ENSP00000477056.1:p.Thr121Ile
ENST00000441880.1:n.114-3227C>T
ENST00000464251.5:c.921C>T	ENSP00000428980.1:n.921C>T
ENST00000466323.5:c.*186C>T	ENSP00000418264.1:n.*186C>T
ENST00000490775.5:n.780C>T
NM_000202.6:c.995C>T	NP_000193.1:p.Thr332Ile
NM_001166550.2:c.725C>T	NP_001160022.1:p.Thr242Ile
NM_006123.4:c.995C>T	NP_006114.1:p.Thr332Ile
NR_104128.1:n.1342C>T
NM_000202.7:c.995C>T	NP_000193.1:p.Thr332Ile
NM_001166550.3:c.725C>T	NP_001160022.1:p.Thr242Ile
NM_000202.8:c.995C>T MANE Select	NP_000193.1:p.Thr332Ile
NM_001166550.4:c.725C>T	NP_001160022.1:p.Thr242Ile
NM_006123.5:c.995C>T	NP_006114.1:p.Thr332Ile
NR_104128.2:n.1294C>T