Canonical Allele Identifier: CA414518695

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148568470T>G (hg19) ; chrX:g.149486939T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486939T>G , CM000685.2:g.149486939T>G	GRCh38
NC_000023.10:g.148568470T>G , CM000685.1:g.148568470T>G	GRCh37
NC_000023.9:g.148376375T>G	NCBI36
NG_011900.3:g.23396A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1166A>C MANE Select	ENSP00000339801.6:p.Gln389Pro
ENST00000651111.1:c.533A>C	ENSP00000498395.1:p.Gln178Pro
ENST00000340855.10:c.1166A>C	ENSP00000339801.6:p.Gln389Pro
ENST00000422081.6:c.533A>C	ENSP00000477056.1:p.Gln178Pro
ENST00000441880.1:n.273A>C
NM_000202.6:c.1166A>C	NP_000193.1:p.Gln389Pro
NM_001166550.2:c.896A>C	NP_001160022.1:p.Gln299Pro
NM_000202.7:c.1166A>C	NP_000193.1:p.Gln389Pro
NM_001166550.3:c.896A>C	NP_001160022.1:p.Gln299Pro
NM_000202.8:c.1166A>C MANE Select	NP_000193.1:p.Gln389Pro
NM_001166550.4:c.896A>C	NP_001160022.1:p.Gln299Pro