Canonical Allele Identifier: CA414520281

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571926T>A (hg19) ; chrX:g.149490395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490395T>A , CM000685.2:g.149490395T>A	GRCh38
NC_000023.10:g.148571926T>A , CM000685.1:g.148571926T>A	GRCh37
NC_000023.9:g.148379831T>A	NCBI36
NG_011900.3:g.19940A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.925A>T MANE Select	ENSP00000339801.6:p.Thr309Ser
ENST00000651111.1:c.292A>T	ENSP00000498395.1:p.Thr98Ser
ENST00000340855.10:c.925A>T	ENSP00000339801.6:p.Thr309Ser
ENST00000370441.8:c.925A>T	ENSP00000359470.4:p.Thr309Ser
ENST00000422081.6:c.292A>T	ENSP00000477056.1:p.Thr98Ser
ENST00000441880.1:n.114-3297A>T
ENST00000464251.5:c.851A>T	ENSP00000428980.1:n.851A>T
ENST00000466323.5:c.*116A>T	ENSP00000418264.1:n.*116A>T
ENST00000490775.5:n.710A>T
NM_000202.6:c.925A>T	NP_000193.1:p.Thr309Ser
NM_001166550.2:c.655A>T	NP_001160022.1:p.Thr219Ser
NM_006123.4:c.925A>T	NP_006114.1:p.Thr309Ser
NR_104128.1:n.1272A>T
NM_000202.7:c.925A>T	NP_000193.1:p.Thr309Ser
NM_001166550.3:c.655A>T	NP_001160022.1:p.Thr219Ser
NM_000202.8:c.925A>T MANE Select	NP_000193.1:p.Thr309Ser
NM_001166550.4:c.655A>T	NP_001160022.1:p.Thr219Ser
NM_006123.5:c.925A>T	NP_006114.1:p.Thr309Ser
NR_104128.2:n.1224A>T