Canonical Allele Identifier: CA519057744

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148571963G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490432G>A , CM000685.2:g.149490432G>A	GRCh38
NC_000023.10:g.148571963G>A , CM000685.1:g.148571963G>A	GRCh37
NC_000023.9:g.148379868G>A	NCBI36
NG_011900.3:g.19903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.888C>T MANE Select	ENSP00000339801.6:p.Ile296=
ENST00000651111.1:c.255C>T	ENSP00000498395.1:p.Ile85=
ENST00000340855.10:c.888C>T	ENSP00000339801.6:p.Ile296=
ENST00000370441.8:c.888C>T	ENSP00000359470.4:p.Ile296=
ENST00000422081.6:c.255C>T	ENSP00000477056.1:p.Ile85=
ENST00000441880.1:n.114-3334C>T
ENST00000464251.5:c.814C>T	ENSP00000428980.1:n.814C>T
ENST00000466323.5:c.*79C>T	ENSP00000418264.1:n.*79C>T
ENST00000490775.5:n.673C>T
NM_000202.6:c.888C>T	NP_000193.1:p.Ile296=
NM_001166550.2:c.618C>T	NP_001160022.1:p.Ile206=
NM_006123.4:c.888C>T	NP_006114.1:p.Ile296=
NR_104128.1:n.1235C>T
NM_000202.7:c.888C>T	NP_000193.1:p.Ile296=
NM_001166550.3:c.618C>T	NP_001160022.1:p.Ile206=
NM_000202.8:c.888C>T MANE Select	NP_000193.1:p.Ile296=
NM_001166550.4:c.618C>T	NP_001160022.1:p.Ile206=
NM_006123.5:c.888C>T	NP_006114.1:p.Ile296=
NR_104128.2:n.1187C>T