Canonical Allele Identifier: CA414522464

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579775C>T (hg19) ; chrX:g.149498244C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498244C>T , CM000685.2:g.149498244C>T	GRCh38
NC_000023.10:g.148579775C>T , CM000685.1:g.148579775C>T	GRCh37
NC_000023.9:g.148387680C>T	NCBI36
NG_011900.3:g.12091G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.571G>A MANE Select	ENSP00000339801.6:p.Val191Ile
ENST00000651111.1:c.-63G>A	ENSP00000498395.1:n.-63G>A
ENST00000340855.10:c.571G>A	ENSP00000339801.6:p.Val191Ile
ENST00000370441.8:c.571G>A	ENSP00000359470.4:p.Val191Ile
ENST00000422081.6:c.-63G>A	ENSP00000477056.1:n.-63G>A
ENST00000441880.1:n.114-11146G>A
ENST00000464251.5:c.497G>A	ENSP00000428980.1:n.497G>A
ENST00000466019.1:n.23G>A
ENST00000466323.5:c.571G>A	ENSP00000418264.1:p.Val191Ile
ENST00000490775.5:n.356G>A
ENST00000523759.5:n.685G>A
NM_000202.6:c.571G>A	NP_000193.1:p.Val191Ile
NM_001166550.2:c.301G>A	NP_001160022.1:p.Val101Ile
NM_006123.4:c.571G>A	NP_006114.1:p.Val191Ile
NR_104128.1:n.788G>A
NM_000202.7:c.571G>A	NP_000193.1:p.Val191Ile
NM_001166550.3:c.301G>A	NP_001160022.1:p.Val101Ile
NM_000202.8:c.571G>A MANE Select	NP_000193.1:p.Val191Ile
NM_001166550.4:c.301G>A	NP_001160022.1:p.Val101Ile
NM_006123.5:c.571G>A	NP_006114.1:p.Val191Ile
NR_104128.2:n.740G>A