Canonical Allele Identifier: CA414526253

Gene: IDS

Linked Data

• ClinVar Variation Id: 642353
• ClinVar RCV Id: RCV000795807
• dbSNP Id: rs1602748386
• MyVariant Identifiers: chrX:g.148584929C>G (hg19) ; chrX:g.149503399C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503399C>G , CM000685.2:g.149503399C>G	GRCh38
NC_000023.10:g.148584929C>G , CM000685.1:g.148584929C>G	GRCh37
NC_000023.9:g.148392834C>G	NCBI36
NG_011900.3:g.6936G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.331G>C MANE Select	ENSP00000339801.6:p.Val111Leu
ENST00000651111.1:c.-215-2362G>C	ENSP00000498395.1:n.-215-2362G>C
ENST00000340855.10:c.331G>C	ENSP00000339801.6:p.Val111Leu
ENST00000370441.8:c.331G>C	ENSP00000359470.4:p.Val111Leu
ENST00000422081.6:c.-215-2362G>C	ENSP00000477056.1:n.-215-2362G>C
ENST00000427113.2:n.770-1176G>C
ENST00000428056.6:c.331G>C	ENSP00000390241.2:p.Val111Leu
ENST00000441880.1:n.114-16301G>C
ENST00000464251.5:c.154G>C	ENSP00000428980.1:p.Val52Leu
ENST00000466323.5:c.331G>C	ENSP00000418264.1:p.Val111Leu
ENST00000523759.5:n.533-2362G>C
NM_000202.6:c.331G>C	NP_000193.1:p.Val111Leu
NM_001166550.2:c.61G>C	NP_001160022.1:p.Val21Leu
NM_006123.4:c.331G>C	NP_006114.1:p.Val111Leu
NR_104128.1:n.548G>C
NM_000202.7:c.331G>C	NP_000193.1:p.Val111Leu
NM_001166550.3:c.61G>C	NP_001160022.1:p.Val21Leu
NM_000202.8:c.331G>C MANE Select	NP_000193.1:p.Val111Leu
NM_001166550.4:c.61G>C	NP_001160022.1:p.Val21Leu
NM_006123.5:c.331G>C	NP_006114.1:p.Val111Leu
NR_104128.2:n.500G>C