Canonical Allele Identifier: CA414520301

Gene: IDS

Linked Data

• ClinVar Variation Id: 1065311
• ClinVar RCV Id: RCV001375842
• dbSNP Id: rs2124020573
• MyVariant Identifiers: chrX:g.148571929C>G (hg19) ; chrX:g.149490398C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490398C>G , CM000685.2:g.149490398C>G	GRCh38
NC_000023.10:g.148571929C>G , CM000685.1:g.148571929C>G	GRCh37
NC_000023.9:g.148379834C>G	NCBI36
NG_011900.3:g.19937G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.922G>C MANE Select	ENSP00000339801.6:p.Asp308His
ENST00000651111.1:c.289G>C	ENSP00000498395.1:p.Asp97His
ENST00000340855.10:c.922G>C	ENSP00000339801.6:p.Asp308His
ENST00000370441.8:c.922G>C	ENSP00000359470.4:p.Asp308His
ENST00000422081.6:c.289G>C	ENSP00000477056.1:p.Asp97His
ENST00000441880.1:n.114-3300G>C
ENST00000464251.5:c.848G>C	ENSP00000428980.1:n.848G>C
ENST00000466323.5:c.*113G>C	ENSP00000418264.1:n.*113G>C
ENST00000490775.5:n.707G>C
NM_000202.6:c.922G>C	NP_000193.1:p.Asp308His
NM_001166550.2:c.652G>C	NP_001160022.1:p.Asp218His
NM_006123.4:c.922G>C	NP_006114.1:p.Asp308His
NR_104128.1:n.1269G>C
NM_000202.7:c.922G>C	NP_000193.1:p.Asp308His
NM_001166550.3:c.652G>C	NP_001160022.1:p.Asp218His
NM_000202.8:c.922G>C MANE Select	NP_000193.1:p.Asp308His
NM_001166550.4:c.652G>C	NP_001160022.1:p.Asp218His
NM_006123.5:c.922G>C	NP_006114.1:p.Asp308His
NR_104128.2:n.1221G>C