Canonical Allele Identifier: CA519058407

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148579788C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498257C>G , CM000685.2:g.149498257C>G	GRCh38
NC_000023.10:g.148579788C>G , CM000685.1:g.148579788C>G	GRCh37
NC_000023.9:g.148387693C>G	NCBI36
NG_011900.3:g.12078G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.558G>C MANE Select	ENSP00000339801.6:p.Val186=
ENST00000651111.1:c.-76G>C	ENSP00000498395.1:n.-76G>C
ENST00000340855.10:c.558G>C	ENSP00000339801.6:p.Val186=
ENST00000370441.8:c.558G>C	ENSP00000359470.4:p.Val186=
ENST00000422081.6:c.-76G>C	ENSP00000477056.1:n.-76G>C
ENST00000441880.1:n.114-11159G>C
ENST00000464251.5:c.484G>C	ENSP00000428980.1:n.484G>C
ENST00000466019.1:n.10G>C
ENST00000466323.5:c.558G>C	ENSP00000418264.1:p.Val186=
ENST00000490775.5:n.343G>C
ENST00000523759.5:n.672G>C
NM_000202.6:c.558G>C	NP_000193.1:p.Val186=
NM_001166550.2:c.288G>C	NP_001160022.1:p.Val96=
NM_006123.4:c.558G>C	NP_006114.1:p.Val186=
NR_104128.1:n.775G>C
NM_000202.7:c.558G>C	NP_000193.1:p.Val186=
NM_001166550.3:c.288G>C	NP_001160022.1:p.Val96=
NM_000202.8:c.558G>C MANE Select	NP_000193.1:p.Val186=
NM_001166550.4:c.288G>C	NP_001160022.1:p.Val96=
NM_006123.5:c.558G>C	NP_006114.1:p.Val186=
NR_104128.2:n.727G>C