Canonical Allele Identifier: CA519057668

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571855G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490324G>A , CM000685.2:g.149490324G>A	GRCh38
NC_000023.10:g.148571855G>A , CM000685.1:g.148571855G>A	GRCh37
NC_000023.9:g.148379760G>A	NCBI36
NG_011900.3:g.20011C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.996C>T MANE Select	ENSP00000339801.6:p.Thr332=
ENST00000651111.1:c.363C>T	ENSP00000498395.1:p.Thr121=
ENST00000340855.10:c.996C>T	ENSP00000339801.6:p.Thr332=
ENST00000370441.8:c.996C>T	ENSP00000359470.4:p.Thr332=
ENST00000422081.6:c.363C>T	ENSP00000477056.1:p.Thr121=
ENST00000441880.1:n.114-3226C>T
ENST00000464251.5:c.922C>T	ENSP00000428980.1:n.922C>T
ENST00000466323.5:c.*187C>T	ENSP00000418264.1:n.*187C>T
ENST00000490775.5:n.781C>T
NM_000202.6:c.996C>T	NP_000193.1:p.Thr332=
NM_001166550.2:c.726C>T	NP_001160022.1:p.Thr242=
NM_006123.4:c.996C>T	NP_006114.1:p.Thr332=
NR_104128.1:n.1343C>T
NM_000202.7:c.996C>T	NP_000193.1:p.Thr332=
NM_001166550.3:c.726C>T	NP_001160022.1:p.Thr242=
NM_000202.8:c.996C>T MANE Select	NP_000193.1:p.Thr332=
NM_001166550.4:c.726C>T	NP_001160022.1:p.Thr242=
NM_006123.5:c.996C>T	NP_006114.1:p.Thr332=
NR_104128.2:n.1295C>T