Canonical Allele Identifier: CA414522540

Gene: IDS

Linked Data

• ClinVar Variation Id: 2576186
• ClinVar RCV Id: RCV003322247
• MyVariant Identifiers: chrX:g.148579810T>C (hg19) ; chrX:g.149498279T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498279T>C , CM000685.2:g.149498279T>C	GRCh38
NC_000023.10:g.148579810T>C , CM000685.1:g.148579810T>C	GRCh37
NC_000023.9:g.148387715T>C	NCBI36
NG_011900.3:g.12056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.536A>G MANE Select	ENSP00000339801.6:p.His179Arg
ENST00000651111.1:c.-98A>G	ENSP00000498395.1:n.-98A>G
ENST00000340855.10:c.536A>G	ENSP00000339801.6:p.His179Arg
ENST00000370441.8:c.536A>G	ENSP00000359470.4:p.His179Arg
ENST00000422081.6:c.-98A>G	ENSP00000477056.1:n.-98A>G
ENST00000441880.1:n.114-11181A>G
ENST00000464251.5:c.462A>G	ENSP00000428980.1:n.462A>G
ENST00000466323.5:c.536A>G	ENSP00000418264.1:p.His179Arg
ENST00000490775.5:n.321A>G
ENST00000523759.5:n.650A>G
NM_000202.6:c.536A>G	NP_000193.1:p.His179Arg
NM_001166550.2:c.266A>G	NP_001160022.1:p.His89Arg
NM_006123.4:c.536A>G	NP_006114.1:p.His179Arg
NR_104128.1:n.753A>G
NM_000202.7:c.536A>G	NP_000193.1:p.His179Arg
NM_001166550.3:c.266A>G	NP_001160022.1:p.His89Arg
NM_000202.8:c.536A>G MANE Select	NP_000193.1:p.His179Arg
NM_001166550.4:c.266A>G	NP_001160022.1:p.His89Arg
NM_006123.5:c.536A>G	NP_006114.1:p.His179Arg
NR_104128.2:n.705A>G