Canonical Allele Identifier: CA337036613

Gene: IDS

Linked Data

• dbSNP Id: rs193302914
• MyVariant Identifiers: chrX:g.148582532C>A (hg19) ; chrX:g.149501001C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149501001C>A , CM000685.2:g.149501001C>A	GRCh38
NC_000023.10:g.148582532C>A , CM000685.1:g.148582532C>A	GRCh37
NC_000023.9:g.148390437C>A	NCBI36
NG_011900.3:g.9334G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.455G>T MANE Select	ENSP00000339801.6:p.Ser152Ile
ENST00000651111.1:c.-179G>T	ENSP00000498395.1:n.-179G>T
ENST00000340855.10:c.455G>T	ENSP00000339801.6:p.Ser152Ile
ENST00000370441.8:c.455G>T	ENSP00000359470.4:p.Ser152Ile
ENST00000422081.6:c.-179G>T	ENSP00000477056.1:n.-179G>T
ENST00000441880.1:n.114-13903G>T
ENST00000464251.5:c.381G>T	ENSP00000428980.1:n.381G>T
ENST00000466323.5:c.455G>T	ENSP00000418264.1:p.Ser152Ile
ENST00000490775.5:n.114G>T
ENST00000523759.5:n.569G>T
NM_000202.6:c.455G>T	NP_000193.1:p.Ser152Ile
NM_001166550.2:c.185G>T	NP_001160022.1:p.Ser62Ile
NM_006123.4:c.455G>T	NP_006114.1:p.Ser152Ile
NR_104128.1:n.672G>T
NM_000202.7:c.455G>T	NP_000193.1:p.Ser152Ile
NM_001166550.3:c.185G>T	NP_001160022.1:p.Ser62Ile
NM_000202.8:c.455G>T MANE Select	NP_000193.1:p.Ser152Ile
NM_001166550.4:c.185G>T	NP_001160022.1:p.Ser62Ile
NM_006123.5:c.455G>T	NP_006114.1:p.Ser152Ile
NR_104128.2:n.624G>T