Canonical Allele Identifier: CA519058380

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579761G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498230G>C , CM000685.2:g.149498230G>C	GRCh38
NC_000023.10:g.148579761G>C , CM000685.1:g.148579761G>C	GRCh37
NC_000023.9:g.148387666G>C	NCBI36
NG_011900.3:g.12105C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.585C>G MANE Select	ENSP00000339801.6:p.Thr195=
ENST00000651111.1:c.-49C>G	ENSP00000498395.1:n.-49C>G
ENST00000340855.10:c.585C>G	ENSP00000339801.6:p.Thr195=
ENST00000370441.8:c.585C>G	ENSP00000359470.4:p.Thr195=
ENST00000422081.6:c.-49C>G	ENSP00000477056.1:n.-49C>G
ENST00000441880.1:n.114-11132C>G
ENST00000464251.5:c.511C>G	ENSP00000428980.1:n.511C>G
ENST00000466019.1:n.37C>G
ENST00000466323.5:c.585C>G	ENSP00000418264.1:p.Thr195=
ENST00000490775.5:n.370C>G
ENST00000523759.5:n.699C>G
NM_000202.6:c.585C>G	NP_000193.1:p.Thr195=
NM_001166550.2:c.315C>G	NP_001160022.1:p.Thr105=
NM_006123.4:c.585C>G	NP_006114.1:p.Thr195=
NR_104128.1:n.802C>G
NM_000202.7:c.585C>G	NP_000193.1:p.Thr195=
NM_001166550.3:c.315C>G	NP_001160022.1:p.Thr105=
NM_000202.8:c.585C>G MANE Select	NP_000193.1:p.Thr195=
NM_001166550.4:c.315C>G	NP_001160022.1:p.Thr105=
NM_006123.5:c.585C>G	NP_006114.1:p.Thr195=
NR_104128.2:n.754C>G