Canonical Allele Identifier: CA519058390

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579773A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498242A>G , CM000685.2:g.149498242A>G	GRCh38
NC_000023.10:g.148579773A>G , CM000685.1:g.148579773A>G	GRCh37
NC_000023.9:g.148387678A>G	NCBI36
NG_011900.3:g.12093T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.573T>C MANE Select	ENSP00000339801.6:p.Val191=
ENST00000651111.1:c.-61T>C	ENSP00000498395.1:n.-61T>C
ENST00000340855.10:c.573T>C	ENSP00000339801.6:p.Val191=
ENST00000370441.8:c.573T>C	ENSP00000359470.4:p.Val191=
ENST00000422081.6:c.-61T>C	ENSP00000477056.1:n.-61T>C
ENST00000441880.1:n.114-11144T>C
ENST00000464251.5:c.499T>C	ENSP00000428980.1:n.499T>C
ENST00000466019.1:n.25T>C
ENST00000466323.5:c.573T>C	ENSP00000418264.1:p.Val191=
ENST00000490775.5:n.358T>C
ENST00000523759.5:n.687T>C
NM_000202.6:c.573T>C	NP_000193.1:p.Val191=
NM_001166550.2:c.303T>C	NP_001160022.1:p.Val101=
NM_006123.4:c.573T>C	NP_006114.1:p.Val191=
NR_104128.1:n.790T>C
NM_000202.7:c.573T>C	NP_000193.1:p.Val191=
NM_001166550.3:c.303T>C	NP_001160022.1:p.Val101=
NM_000202.8:c.573T>C MANE Select	NP_000193.1:p.Val191=
NM_001166550.4:c.303T>C	NP_001160022.1:p.Val101=
NM_006123.5:c.573T>C	NP_006114.1:p.Val191=
NR_104128.2:n.742T>C