Canonical Allele Identifier: CA519057978

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148577945T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496414T>G , CM000685.2:g.149496414T>G	GRCh38
NC_000023.10:g.148577945T>G , CM000685.1:g.148577945T>G	GRCh37
NC_000023.9:g.148385850T>G	NCBI36
NG_011900.3:g.13921A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.811A>C MANE Select	ENSP00000339801.6:p.Arg271=
ENST00000651111.1:c.178A>C	ENSP00000498395.1:p.Arg60=
ENST00000340855.10:c.811A>C	ENSP00000339801.6:p.Arg271=
ENST00000370441.8:c.811A>C	ENSP00000359470.4:p.Arg271=
ENST00000422081.6:c.178A>C	ENSP00000477056.1:p.Arg60=
ENST00000441880.1:n.114-9316A>C
ENST00000464251.5:c.737A>C	ENSP00000428980.1:n.737A>C
ENST00000466019.1:n.263A>C
ENST00000466323.5:c.811A>C	ENSP00000418264.1:p.Arg271=
ENST00000490775.5:n.596A>C
NM_000202.6:c.811A>C	NP_000193.1:p.Arg271=
NM_001166550.2:c.541A>C	NP_001160022.1:p.Arg181=
NM_006123.4:c.811A>C	NP_006114.1:p.Arg271=
NR_104128.1:n.1028A>C
NM_000202.7:c.811A>C	NP_000193.1:p.Arg271=
NM_001166550.3:c.541A>C	NP_001160022.1:p.Arg181=
NM_000202.8:c.811A>C MANE Select	NP_000193.1:p.Arg271=
NM_001166550.4:c.541A>C	NP_001160022.1:p.Arg181=
NM_006123.5:c.811A>C	NP_006114.1:p.Arg271=
NR_104128.2:n.980A>C