Canonical Allele Identifier: CA414522217

Gene: IDS

Linked Data

• ClinVar Variation Id: 2430992
• ClinVar RCV Id: RCV003129525
• COSMIC: COSM4887371 ; COSM4887372 ; COSM4887373
• MyVariant Identifiers: chrX:g.148579679C>A (hg19) ; chrX:g.149498148C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498148C>A , CM000685.2:g.149498148C>A	GRCh38
NC_000023.10:g.148579679C>A , CM000685.1:g.148579679C>A	GRCh37
NC_000023.9:g.148387584C>A	NCBI36
NG_011900.3:g.12187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.667G>T MANE Select	ENSP00000339801.6:p.Val223Phe
ENST00000651111.1:c.34G>T	ENSP00000498395.1:p.Val12Phe
ENST00000340855.10:c.667G>T	ENSP00000339801.6:p.Val223Phe
ENST00000370441.8:c.667G>T	ENSP00000359470.4:p.Val223Phe
ENST00000422081.6:c.34G>T	ENSP00000477056.1:p.Val12Phe
ENST00000441880.1:n.114-11050G>T
ENST00000464251.5:c.593G>T	ENSP00000428980.1:n.593G>T
ENST00000466019.1:n.119G>T
ENST00000466323.5:c.667G>T	ENSP00000418264.1:p.Val223Phe
ENST00000490775.5:n.452G>T
NM_000202.6:c.667G>T	NP_000193.1:p.Val223Phe
NM_001166550.2:c.397G>T	NP_001160022.1:p.Val133Phe
NM_006123.4:c.667G>T	NP_006114.1:p.Val223Phe
NR_104128.1:n.884G>T
NM_000202.7:c.667G>T	NP_000193.1:p.Val223Phe
NM_001166550.3:c.397G>T	NP_001160022.1:p.Val133Phe
NM_000202.8:c.667G>T MANE Select	NP_000193.1:p.Val223Phe
NM_001166550.4:c.397G>T	NP_001160022.1:p.Val133Phe
NM_006123.5:c.667G>T	NP_006114.1:p.Val223Phe
NR_104128.2:n.836G>T