Canonical Allele Identifier: CA519057686

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571879G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490348G>A , CM000685.2:g.149490348G>A	GRCh38
NC_000023.10:g.148571879G>A , CM000685.1:g.148571879G>A	GRCh37
NC_000023.9:g.148379784G>A	NCBI36
NG_011900.3:g.19987C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.972C>T MANE Select	ENSP00000339801.6:p.Ala324=
ENST00000651111.1:c.339C>T	ENSP00000498395.1:p.Ala113=
ENST00000340855.10:c.972C>T	ENSP00000339801.6:p.Ala324=
ENST00000370441.8:c.972C>T	ENSP00000359470.4:p.Ala324=
ENST00000422081.6:c.339C>T	ENSP00000477056.1:p.Ala113=
ENST00000441880.1:n.114-3250C>T
ENST00000464251.5:c.898C>T	ENSP00000428980.1:n.898C>T
ENST00000466323.5:c.*163C>T	ENSP00000418264.1:n.*163C>T
ENST00000490775.5:n.757C>T
NM_000202.6:c.972C>T	NP_000193.1:p.Ala324=
NM_001166550.2:c.702C>T	NP_001160022.1:p.Ala234=
NM_006123.4:c.972C>T	NP_006114.1:p.Ala324=
NR_104128.1:n.1319C>T
NM_000202.7:c.972C>T	NP_000193.1:p.Ala324=
NM_001166550.3:c.702C>T	NP_001160022.1:p.Ala234=
NM_000202.8:c.972C>T MANE Select	NP_000193.1:p.Ala324=
NM_001166550.4:c.702C>T	NP_001160022.1:p.Ala234=
NM_006123.5:c.972C>T	NP_006114.1:p.Ala324=
NR_104128.2:n.1271C>T