Canonical Allele Identifier: CA519062160

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148585735A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149504205A>G , CM000685.2:g.149504205A>G	GRCh38
NC_000023.10:g.148585735A>G , CM000685.1:g.148585735A>G	GRCh37
NC_000023.9:g.148393639A>G	NCBI36
NG_011900.3:g.6130T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.192T>C MANE Select	ENSP00000339801.6:p.Ile64=
ENST00000651111.1:c.-215-3168T>C	ENSP00000498395.1:n.-215-3168T>C
ENST00000340855.10:c.192T>C	ENSP00000339801.6:p.Ile64=
ENST00000370441.8:c.192T>C	ENSP00000359470.4:p.Ile64=
ENST00000422081.6:c.-215-3168T>C	ENSP00000477056.1:n.-215-3168T>C
ENST00000427113.2:n.770-1982T>C
ENST00000428056.6:c.192T>C	ENSP00000390241.2:p.Ile64=
ENST00000441880.1:n.114-17107T>C
ENST00000464251.5:c.15T>C	ENSP00000428980.1:p.Ile5=
ENST00000466323.5:c.192T>C	ENSP00000418264.1:p.Ile64=
ENST00000521702.1:c.192T>C	ENSP00000429745.1:p.Ile64=
ENST00000523759.5:n.533-3168T>C
NM_000202.6:c.192T>C	NP_000193.1:p.Ile64=
NM_001166550.2:c.-35T>C	NP_001160022.1:n.-35T>C
NM_006123.4:c.192T>C	NP_006114.1:p.Ile64=
NR_104128.1:n.409T>C
NM_000202.7:c.192T>C	NP_000193.1:p.Ile64=
NM_001166550.3:c.-35T>C	NP_001160022.1:n.-35T>C
NM_000202.8:c.192T>C MANE Select	NP_000193.1:p.Ile64=
NM_001166550.4:c.-35T>C	NP_001160022.1:n.-35T>C
NM_006123.5:c.192T>C	NP_006114.1:p.Ile64=
NR_104128.2:n.361T>C