Canonical Allele Identifier: CA414518389

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148564629T>G (hg19) ; chrX:g.149483098T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483098T>G , CM000685.2:g.149483098T>G	GRCh38
NC_000023.10:g.148564629T>G , CM000685.1:g.148564629T>G	GRCh37
NC_000023.9:g.148372534T>G	NCBI36
NG_011900.3:g.27237A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1301A>C MANE Select	ENSP00000339801.6:p.Glu434Ala
ENST00000651111.1:c.668A>C	ENSP00000498395.1:p.Glu223Ala
ENST00000340855.10:c.1301A>C	ENSP00000339801.6:p.Glu434Ala
ENST00000422081.6:c.668A>C	ENSP00000477056.1:p.Glu223Ala
ENST00000441880.1:n.408A>C
NM_000202.6:c.1301A>C	NP_000193.1:p.Glu434Ala
NM_001166550.2:c.1031A>C	NP_001160022.1:p.Glu344Ala
NM_000202.7:c.1301A>C	NP_000193.1:p.Glu434Ala
NM_001166550.3:c.1031A>C	NP_001160022.1:p.Glu344Ala
NM_000202.8:c.1301A>C MANE Select	NP_000193.1:p.Glu434Ala
NM_001166550.4:c.1031A>C	NP_001160022.1:p.Glu344Ala