Canonical Allele Identifier: CA414519855

Gene: IDS

Linked Data

• ClinVar Variation Id: 1459022
• ClinVar RCV Id: RCV001949645
• dbSNP Id: rs104894853
• MyVariant Identifiers: chrX:g.148571853G>C (hg19) ; chrX:g.149490322G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490322G>C , CM000685.2:g.149490322G>C	GRCh38
NC_000023.10:g.148571853G>C , CM000685.1:g.148571853G>C	GRCh37
NC_000023.9:g.148379758G>C	NCBI36
NG_011900.3:g.20013C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.998C>G MANE Select	ENSP00000339801.6:p.Ser333Trp
ENST00000651111.1:c.365C>G	ENSP00000498395.1:p.Ser122Trp
ENST00000340855.10:c.998C>G	ENSP00000339801.6:p.Ser333Trp
ENST00000370441.8:c.998C>G	ENSP00000359470.4:p.Ser333Trp
ENST00000422081.6:c.365C>G	ENSP00000477056.1:p.Ser122Trp
ENST00000441880.1:n.114-3224C>G
ENST00000464251.5:c.924C>G	ENSP00000428980.1:n.924C>G
ENST00000466323.5:c.*189C>G	ENSP00000418264.1:n.*189C>G
ENST00000490775.5:n.783C>G
NM_000202.6:c.998C>G	NP_000193.1:p.Ser333Trp
NM_001166550.2:c.728C>G	NP_001160022.1:p.Ser243Trp
NM_006123.4:c.998C>G	NP_006114.1:p.Ser333Trp
NR_104128.1:n.1345C>G
NM_000202.7:c.998C>G	NP_000193.1:p.Ser333Trp
NM_001166550.3:c.728C>G	NP_001160022.1:p.Ser243Trp
NM_000202.8:c.998C>G MANE Select	NP_000193.1:p.Ser333Trp
NM_001166550.4:c.728C>G	NP_001160022.1:p.Ser243Trp
NM_006123.5:c.998C>G	NP_006114.1:p.Ser333Trp
NR_104128.2:n.1297C>G