Canonical Allele Identifier: CA414525586

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148584853A>T (hg19) ; chrX:g.149503323A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503323A>T , CM000685.2:g.149503323A>T	GRCh38
NC_000023.10:g.148584853A>T , CM000685.1:g.148584853A>T	GRCh37
NC_000023.9:g.148392758A>T	NCBI36
NG_011900.3:g.7012T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.407T>A MANE Select	ENSP00000339801.6:p.Val136Asp
ENST00000651111.1:c.-215-2286T>A	ENSP00000498395.1:n.-215-2286T>A
ENST00000340855.10:c.407T>A	ENSP00000339801.6:p.Val136Asp
ENST00000370441.8:c.407T>A	ENSP00000359470.4:p.Val136Asp
ENST00000422081.6:c.-215-2286T>A	ENSP00000477056.1:n.-215-2286T>A
ENST00000427113.2:n.770-1100T>A
ENST00000428056.6:c.407T>A	ENSP00000390241.2:p.Val136Asp
ENST00000441880.1:n.114-16225T>A
ENST00000464251.5:c.230T>A	ENSP00000428980.1:p.Val77Asp
ENST00000466323.5:c.407T>A	ENSP00000418264.1:p.Val136Asp
ENST00000490775.5:n.66T>A
ENST00000523759.5:n.533-2286T>A
NM_000202.6:c.407T>A	NP_000193.1:p.Val136Asp
NM_001166550.2:c.137T>A	NP_001160022.1:p.Val46Asp
NM_006123.4:c.407T>A	NP_006114.1:p.Val136Asp
NR_104128.1:n.624T>A
NM_000202.7:c.407T>A	NP_000193.1:p.Val136Asp
NM_001166550.3:c.137T>A	NP_001160022.1:p.Val46Asp
NM_000202.8:c.407T>A MANE Select	NP_000193.1:p.Val136Asp
NM_001166550.4:c.137T>A	NP_001160022.1:p.Val46Asp
NM_006123.5:c.407T>A	NP_006114.1:p.Val136Asp
NR_104128.2:n.576T>A