Canonical Allele Identifier: CA414525599

Gene: IDS

Linked Data

• dbSNP Id: rs2089495566
• MyVariant Identifiers: chrX:g.148584854C>T (hg19) ; chrX:g.149503324C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503324C>T , CM000685.2:g.149503324C>T	GRCh38
NC_000023.10:g.148584854C>T , CM000685.1:g.148584854C>T	GRCh37
NC_000023.9:g.148392759C>T	NCBI36
NG_011900.3:g.7011G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.406G>A MANE Select	ENSP00000339801.6:p.Val136Ile
ENST00000651111.1:c.-215-2287G>A	ENSP00000498395.1:n.-215-2287G>A
ENST00000340855.10:c.406G>A	ENSP00000339801.6:p.Val136Ile
ENST00000370441.8:c.406G>A	ENSP00000359470.4:p.Val136Ile
ENST00000422081.6:c.-215-2287G>A	ENSP00000477056.1:n.-215-2287G>A
ENST00000427113.2:n.770-1101G>A
ENST00000428056.6:c.406G>A	ENSP00000390241.2:p.Val136Ile
ENST00000441880.1:n.114-16226G>A
ENST00000464251.5:c.229G>A	ENSP00000428980.1:p.Val77Ile
ENST00000466323.5:c.406G>A	ENSP00000418264.1:p.Val136Ile
ENST00000490775.5:n.65G>A
ENST00000523759.5:n.533-2287G>A
NM_000202.6:c.406G>A	NP_000193.1:p.Val136Ile
NM_001166550.2:c.136G>A	NP_001160022.1:p.Val46Ile
NM_006123.4:c.406G>A	NP_006114.1:p.Val136Ile
NR_104128.1:n.623G>A
NM_000202.7:c.406G>A	NP_000193.1:p.Val136Ile
NM_001166550.3:c.136G>A	NP_001160022.1:p.Val46Ile
NM_000202.8:c.406G>A MANE Select	NP_000193.1:p.Val136Ile
NM_001166550.4:c.136G>A	NP_001160022.1:p.Val46Ile
NM_006123.5:c.406G>A	NP_006114.1:p.Val136Ile
NR_104128.2:n.575G>A