Canonical Allele Identifier: CA414526444

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148584947A>T (hg19) ; chrX:g.149503417A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503417A>T , CM000685.2:g.149503417A>T	GRCh38
NC_000023.10:g.148584947A>T , CM000685.1:g.148584947A>T	GRCh37
NC_000023.9:g.148392852A>T	NCBI36
NG_011900.3:g.6918T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.313T>A MANE Select	ENSP00000339801.6:p.Phe105Ile
ENST00000651111.1:c.-215-2380T>A	ENSP00000498395.1:n.-215-2380T>A
ENST00000340855.10:c.313T>A	ENSP00000339801.6:p.Phe105Ile
ENST00000370441.8:c.313T>A	ENSP00000359470.4:p.Phe105Ile
ENST00000422081.6:c.-215-2380T>A	ENSP00000477056.1:n.-215-2380T>A
ENST00000427113.2:n.770-1194T>A
ENST00000428056.6:c.313T>A	ENSP00000390241.2:p.Phe105Ile
ENST00000441880.1:n.114-16319T>A
ENST00000464251.5:c.136T>A	ENSP00000428980.1:p.Phe46Ile
ENST00000466323.5:c.313T>A	ENSP00000418264.1:p.Phe105Ile
ENST00000523759.5:n.533-2380T>A
NM_000202.6:c.313T>A	NP_000193.1:p.Phe105Ile
NM_001166550.2:c.43T>A	NP_001160022.1:p.Phe15Ile
NM_006123.4:c.313T>A	NP_006114.1:p.Phe105Ile
NR_104128.1:n.530T>A
NM_000202.7:c.313T>A	NP_000193.1:p.Phe105Ile
NM_001166550.3:c.43T>A	NP_001160022.1:p.Phe15Ile
NM_000202.8:c.313T>A MANE Select	NP_000193.1:p.Phe105Ile
NM_001166550.4:c.43T>A	NP_001160022.1:p.Phe15Ile
NM_006123.5:c.313T>A	NP_006114.1:p.Phe105Ile
NR_104128.2:n.482T>A