Canonical Allele Identifier: CA414519846

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571851C>A (hg19) ; chrX:g.149490320C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490320C>A , CM000685.2:g.149490320C>A	GRCh38
NC_000023.10:g.148571851C>A , CM000685.1:g.148571851C>A	GRCh37
NC_000023.9:g.148379756C>A	NCBI36
NG_011900.3:g.20015G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1000G>T MANE Select	ENSP00000339801.6:p.Asp334Tyr
ENST00000651111.1:c.367G>T	ENSP00000498395.1:p.Asp123Tyr
ENST00000340855.10:c.1000G>T	ENSP00000339801.6:p.Asp334Tyr
ENST00000370441.8:c.1000G>T	ENSP00000359470.4:p.Asp334Tyr
ENST00000422081.6:c.367G>T	ENSP00000477056.1:p.Asp123Tyr
ENST00000441880.1:n.114-3222G>T
ENST00000464251.5:c.926G>T	ENSP00000428980.1:n.926G>T
ENST00000466323.5:c.*191G>T	ENSP00000418264.1:n.*191G>T
ENST00000490775.5:n.785G>T
NM_000202.6:c.1000G>T	NP_000193.1:p.Asp334Tyr
NM_001166550.2:c.730G>T	NP_001160022.1:p.Asp244Tyr
NM_006123.4:c.1000G>T	NP_006114.1:p.Asp334Tyr
NR_104128.1:n.1347G>T
NM_000202.7:c.1000G>T	NP_000193.1:p.Asp334Tyr
NM_001166550.3:c.730G>T	NP_001160022.1:p.Asp244Tyr
NM_000202.8:c.1000G>T MANE Select	NP_000193.1:p.Asp334Tyr
NM_001166550.4:c.730G>T	NP_001160022.1:p.Asp244Tyr
NM_006123.5:c.1000G>T	NP_006114.1:p.Asp334Tyr
NR_104128.2:n.1299G>T