Canonical Allele Identifier: CA519057967

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148577937C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496406C>A , CM000685.2:g.149496406C>A	GRCh38
NC_000023.10:g.148577937C>A , CM000685.1:g.148577937C>A	GRCh37
NC_000023.9:g.148385842C>A	NCBI36
NG_011900.3:g.13929G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.819G>T MANE Select	ENSP00000339801.6:p.Arg273=
ENST00000651111.1:c.186G>T	ENSP00000498395.1:p.Arg62=
ENST00000340855.10:c.819G>T	ENSP00000339801.6:p.Arg273=
ENST00000370441.8:c.819G>T	ENSP00000359470.4:p.Arg273=
ENST00000422081.6:c.186G>T	ENSP00000477056.1:p.Arg62=
ENST00000441880.1:n.114-9308G>T
ENST00000464251.5:c.745G>T	ENSP00000428980.1:n.745G>T
ENST00000466019.1:n.271G>T
ENST00000466323.5:c.819G>T	ENSP00000418264.1:p.Arg273=
ENST00000490775.5:n.604G>T
NM_000202.6:c.819G>T	NP_000193.1:p.Arg273=
NM_001166550.2:c.549G>T	NP_001160022.1:p.Arg183=
NM_006123.4:c.819G>T	NP_006114.1:p.Arg273=
NR_104128.1:n.1036G>T
NM_000202.7:c.819G>T	NP_000193.1:p.Arg273=
NM_001166550.3:c.549G>T	NP_001160022.1:p.Arg183=
NM_000202.8:c.819G>T MANE Select	NP_000193.1:p.Arg273=
NM_001166550.4:c.549G>T	NP_001160022.1:p.Arg183=
NM_006123.5:c.819G>T	NP_006114.1:p.Arg273=
NR_104128.2:n.988G>T