Canonical Allele Identifier: CA414520558

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571971G>C (hg19) ; chrX:g.149490440G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490440G>C , CM000685.2:g.149490440G>C	GRCh38
NC_000023.10:g.148571971G>C , CM000685.1:g.148571971G>C	GRCh37
NC_000023.9:g.148379876G>C	NCBI36
NG_011900.3:g.19895C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880C>G MANE Select	ENSP00000339801.6:p.Arg294Gly
ENST00000651111.1:c.247C>G	ENSP00000498395.1:p.Arg83Gly
ENST00000340855.10:c.880C>G	ENSP00000339801.6:p.Arg294Gly
ENST00000370441.8:c.880C>G	ENSP00000359470.4:p.Arg294Gly
ENST00000422081.6:c.247C>G	ENSP00000477056.1:p.Arg83Gly
ENST00000441880.1:n.114-3342C>G
ENST00000464251.5:c.806C>G	ENSP00000428980.1:n.806C>G
ENST00000466323.5:c.*71C>G	ENSP00000418264.1:n.*71C>G
ENST00000490775.5:n.665C>G
NM_000202.6:c.880C>G	NP_000193.1:p.Arg294Gly
NM_001166550.2:c.610C>G	NP_001160022.1:p.Arg204Gly
NM_006123.4:c.880C>G	NP_006114.1:p.Arg294Gly
NR_104128.1:n.1227C>G
NM_000202.7:c.880C>G	NP_000193.1:p.Arg294Gly
NM_001166550.3:c.610C>G	NP_001160022.1:p.Arg204Gly
NM_000202.8:c.880C>G MANE Select	NP_000193.1:p.Arg294Gly
NM_001166550.4:c.610C>G	NP_001160022.1:p.Arg204Gly
NM_006123.5:c.880C>G	NP_006114.1:p.Arg294Gly
NR_104128.2:n.1179C>G