Canonical Allele Identifier: CA414522602

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579837G>A (hg19) ; chrX:g.149498306G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498306G>A , CM000685.2:g.149498306G>A	GRCh38
NC_000023.10:g.148579837G>A , CM000685.1:g.148579837G>A	GRCh37
NC_000023.9:g.148387742G>A	NCBI36
NG_011900.3:g.12029C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.509C>T MANE Select	ENSP00000339801.6:p.Thr170Ile
ENST00000651111.1:c.-125C>T	ENSP00000498395.1:n.-125C>T
ENST00000340855.10:c.509C>T	ENSP00000339801.6:p.Thr170Ile
ENST00000370441.8:c.509C>T	ENSP00000359470.4:p.Thr170Ile
ENST00000422081.6:c.-125C>T	ENSP00000477056.1:n.-125C>T
ENST00000441880.1:n.114-11208C>T
ENST00000464251.5:c.435C>T	ENSP00000428980.1:n.435C>T
ENST00000466323.5:c.509C>T	ENSP00000418264.1:p.Thr170Ile
ENST00000490775.5:n.294C>T
ENST00000523759.5:n.623C>T
NM_000202.6:c.509C>T	NP_000193.1:p.Thr170Ile
NM_001166550.2:c.239C>T	NP_001160022.1:p.Thr80Ile
NM_006123.4:c.509C>T	NP_006114.1:p.Thr170Ile
NR_104128.1:n.726C>T
NM_000202.7:c.509C>T	NP_000193.1:p.Thr170Ile
NM_001166550.3:c.239C>T	NP_001160022.1:p.Thr80Ile
NM_000202.8:c.509C>T MANE Select	NP_000193.1:p.Thr170Ile
NM_001166550.4:c.239C>T	NP_001160022.1:p.Thr80Ile
NM_006123.5:c.509C>T	NP_006114.1:p.Thr170Ile
NR_104128.2:n.678C>T