Canonical Allele Identifier: CA414520251

Gene: IDS

Linked Data

• gnomAD v4: X-149490389-C-T
• MyVariant Identifiers: chrX:g.148571920C>T (hg19) ; chrX:g.149490389C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490389C>T , CM000685.2:g.149490389C>T	GRCh38
NC_000023.10:g.148571920C>T , CM000685.1:g.148571920C>T	GRCh37
NC_000023.9:g.148379825C>T	NCBI36
NG_011900.3:g.19946G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000340855.11:c.931G>A MANE Select	ENSP00000339801.6:p.Val311Ile
ENST00000651111.1:c.298G>A	ENSP00000498395.1:p.Val100Ile
ENST00000340855.10:c.931G>A	ENSP00000339801.6:p.Val311Ile
ENST00000370441.8:c.931G>A	ENSP00000359470.4:p.Val311Ile
ENST00000422081.6:c.298G>A	ENSP00000477056.1:p.Val100Ile
ENST00000441880.1:n.114-3291G>A
ENST00000464251.5:c.857G>A	ENSP00000428980.1:n.857G>A
ENST00000466323.5:c.*122G>A	ENSP00000418264.1:n.*122G>A
ENST00000490775.5:n.716G>A
NM_000202.6:c.931G>A	NP_000193.1:p.Val311Ile
NM_001166550.2:c.661G>A	NP_001160022.1:p.Val221Ile
NM_006123.4:c.931G>A	NP_006114.1:p.Val311Ile
NR_104128.1:n.1278G>A
NM_000202.7:c.931G>A	NP_000193.1:p.Val311Ile
NM_001166550.3:c.661G>A	NP_001160022.1:p.Val221Ile
NM_000202.8:c.931G>A MANE Select	NP_000193.1:p.Val311Ile
NM_001166550.4:c.661G>A	NP_001160022.1:p.Val221Ile
NM_006123.5:c.931G>A	NP_006114.1:p.Val311Ile
NR_104128.2:n.1230G>A