Canonical Allele Identifier: CA519057997

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148577958G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496427G>T , CM000685.2:g.149496427G>T	GRCh38
NC_000023.10:g.148577958G>T , CM000685.1:g.148577958G>T	GRCh37
NC_000023.9:g.148385863G>T	NCBI36
NG_011900.3:g.13908C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.798C>A MANE Select	ENSP00000339801.6:p.Pro266=
ENST00000651111.1:c.165C>A	ENSP00000498395.1:p.Pro55=
ENST00000340855.10:c.798C>A	ENSP00000339801.6:p.Pro266=
ENST00000370441.8:c.798C>A	ENSP00000359470.4:p.Pro266=
ENST00000422081.6:c.165C>A	ENSP00000477056.1:p.Pro55=
ENST00000441880.1:n.114-9329C>A
ENST00000464251.5:c.724C>A	ENSP00000428980.1:n.724C>A
ENST00000466019.1:n.250C>A
ENST00000466323.5:c.798C>A	ENSP00000418264.1:p.Pro266=
ENST00000490775.5:n.583C>A
NM_000202.6:c.798C>A	NP_000193.1:p.Pro266=
NM_001166550.2:c.528C>A	NP_001160022.1:p.Pro176=
NM_006123.4:c.798C>A	NP_006114.1:p.Pro266=
NR_104128.1:n.1015C>A
NM_000202.7:c.798C>A	NP_000193.1:p.Pro266=
NM_001166550.3:c.528C>A	NP_001160022.1:p.Pro176=
NM_000202.8:c.798C>A MANE Select	NP_000193.1:p.Pro266=
NM_001166550.4:c.528C>A	NP_001160022.1:p.Pro176=
NM_006123.5:c.798C>A	NP_006114.1:p.Pro266=
NR_104128.2:n.967C>A