Canonical Allele Identifier: CA10537548

Gene: IDS

Linked Data

• ClinVar Variation Id: 1154582
• ClinVar RCV Id: RCV001496618
• dbSNP Id: rs782210625
• ExAC: X:148571922 T / C
• gnomAD v2: X-148571922-T-C
• gnomAD v4: X-149490391-T-C
• MyVariant Identifiers: chrX:g.148571922T>C (hg19) ; chrX:g.149490391T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490391T>C , CM000685.2:g.149490391T>C	GRCh38
NC_000023.10:g.148571922T>C , CM000685.1:g.148571922T>C	GRCh37
NC_000023.9:g.148379827T>C	NCBI36
NG_011900.3:g.19944A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.929A>G MANE Select	ENSP00000339801.6:p.Gln310Arg
ENST00000651111.1:c.296A>G	ENSP00000498395.1:p.Gln99Arg
ENST00000340855.10:c.929A>G	ENSP00000339801.6:p.Gln310Arg
ENST00000370441.8:c.929A>G	ENSP00000359470.4:p.Gln310Arg
ENST00000422081.6:c.296A>G	ENSP00000477056.1:p.Gln99Arg
ENST00000441880.1:n.114-3293A>G
ENST00000464251.5:c.855A>G	ENSP00000428980.1:n.855A>G
ENST00000466323.5:c.*120A>G	ENSP00000418264.1:n.*120A>G
ENST00000490775.5:n.714A>G
NM_000202.6:c.929A>G	NP_000193.1:p.Gln310Arg
NM_001166550.2:c.659A>G	NP_001160022.1:p.Gln220Arg
NM_006123.4:c.929A>G	NP_006114.1:p.Gln310Arg
NR_104128.1:n.1276A>G
NM_000202.7:c.929A>G	NP_000193.1:p.Gln310Arg
NM_001166550.3:c.659A>G	NP_001160022.1:p.Gln220Arg
NM_000202.8:c.929A>G MANE Select	NP_000193.1:p.Gln310Arg
NM_001166550.4:c.659A>G	NP_001160022.1:p.Gln220Arg
NM_006123.5:c.929A>G	NP_006114.1:p.Gln310Arg
NR_104128.2:n.1228A>G