Canonical Allele Identifier: CA414526597

Gene: IDS

Linked Data

• gnomAD v2: X-148584968-C-T
• gnomAD v3: X-149503438-C-T
• gnomAD v4: X-149503438-C-T
• MyVariant Identifiers: chrX:g.148584968C>T (hg19) ; chrX:g.149503438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503438C>T , CM000685.2:g.149503438C>T	GRCh38
NC_000023.10:g.148584968C>T , CM000685.1:g.148584968C>T	GRCh37
NC_000023.9:g.148392873C>T	NCBI36
NG_011900.3:g.6897G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.292G>A MANE Select	ENSP00000339801.6:p.Asp98Asn
ENST00000651111.1:c.-215-2401G>A	ENSP00000498395.1:n.-215-2401G>A
ENST00000340855.10:c.292G>A	ENSP00000339801.6:p.Asp98Asn
ENST00000370441.8:c.292G>A	ENSP00000359470.4:p.Asp98Asn
ENST00000422081.6:c.-215-2401G>A	ENSP00000477056.1:n.-215-2401G>A
ENST00000427113.2:n.770-1215G>A
ENST00000428056.6:c.292G>A	ENSP00000390241.2:p.Asp98Asn
ENST00000441880.1:n.114-16340G>A
ENST00000464251.5:c.115G>A	ENSP00000428980.1:p.Asp39Asn
ENST00000466323.5:c.292G>A	ENSP00000418264.1:p.Asp98Asn
ENST00000523759.5:n.533-2401G>A
NM_000202.6:c.292G>A	NP_000193.1:p.Asp98Asn
NM_001166550.2:c.22G>A	NP_001160022.1:p.Asp8Asn
NM_006123.4:c.292G>A	NP_006114.1:p.Asp98Asn
NR_104128.1:n.509G>A
NM_000202.7:c.292G>A	NP_000193.1:p.Asp98Asn
NM_001166550.3:c.22G>A	NP_001160022.1:p.Asp8Asn
NM_000202.8:c.292G>A MANE Select	NP_000193.1:p.Asp98Asn
NM_001166550.4:c.22G>A	NP_001160022.1:p.Asp8Asn
NM_006123.5:c.292G>A	NP_006114.1:p.Asp98Asn
NR_104128.2:n.461G>A