Canonical Allele Identifier: CA519057704

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571900A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490369A>T , CM000685.2:g.149490369A>T	GRCh38
NC_000023.10:g.148571900A>T , CM000685.1:g.148571900A>T	GRCh37
NC_000023.9:g.148379805A>T	NCBI36
NG_011900.3:g.19966T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.951T>A MANE Select	ENSP00000339801.6:p.Ala317=
ENST00000651111.1:c.318T>A	ENSP00000498395.1:p.Ala106=
ENST00000340855.10:c.951T>A	ENSP00000339801.6:p.Ala317=
ENST00000370441.8:c.951T>A	ENSP00000359470.4:p.Ala317=
ENST00000422081.6:c.318T>A	ENSP00000477056.1:p.Ala106=
ENST00000441880.1:n.114-3271T>A
ENST00000464251.5:c.877T>A	ENSP00000428980.1:n.877T>A
ENST00000466323.5:c.*142T>A	ENSP00000418264.1:n.*142T>A
ENST00000490775.5:n.736T>A
NM_000202.6:c.951T>A	NP_000193.1:p.Ala317=
NM_001166550.2:c.681T>A	NP_001160022.1:p.Ala227=
NM_006123.4:c.951T>A	NP_006114.1:p.Ala317=
NR_104128.1:n.1298T>A
NM_000202.7:c.951T>A	NP_000193.1:p.Ala317=
NM_001166550.3:c.681T>A	NP_001160022.1:p.Ala227=
NM_000202.8:c.951T>A MANE Select	NP_000193.1:p.Ala317=
NM_001166550.4:c.681T>A	NP_001160022.1:p.Ala227=
NM_006123.5:c.951T>A	NP_006114.1:p.Ala317=
NR_104128.2:n.1250T>A