Canonical Allele Identifier: CA414518705

Gene: IDS

Linked Data

• gnomAD v4: X-149486945-G-A
• MyVariant Identifiers: chrX:g.148568476G>A (hg19) ; chrX:g.149486945G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486945G>A , CM000685.2:g.149486945G>A	GRCh38
NC_000023.10:g.148568476G>A , CM000685.1:g.148568476G>A	GRCh37
NC_000023.9:g.148376381G>A	NCBI36
NG_011900.3:g.23390C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1160C>T MANE Select	ENSP00000339801.6:p.Ala387Val
ENST00000651111.1:c.527C>T	ENSP00000498395.1:p.Ala176Val
ENST00000340855.10:c.1160C>T	ENSP00000339801.6:p.Ala387Val
ENST00000422081.6:c.527C>T	ENSP00000477056.1:p.Ala176Val
ENST00000441880.1:n.267C>T
NM_000202.6:c.1160C>T	NP_000193.1:p.Ala387Val
NM_001166550.2:c.890C>T	NP_001160022.1:p.Ala297Val
NM_000202.7:c.1160C>T	NP_000193.1:p.Ala387Val
NM_001166550.3:c.890C>T	NP_001160022.1:p.Ala297Val
NM_000202.8:c.1160C>T MANE Select	NP_000193.1:p.Ala387Val
NM_001166550.4:c.890C>T	NP_001160022.1:p.Ala297Val