Canonical Allele Identifier: CA519173878

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148564529G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149482998G>A , CM000685.2:g.149482998G>A	GRCh38
NC_000023.10:g.148564529G>A , CM000685.1:g.148564529G>A	GRCh37
NC_000023.9:g.148372434G>A	NCBI36
NG_011900.3:g.27337C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1401C>T MANE Select	ENSP00000339801.6:p.Pro467=
ENST00000651111.1:c.768C>T	ENSP00000498395.1:p.Pro256=
ENST00000340855.10:c.1401C>T	ENSP00000339801.6:p.Pro467=
ENST00000422081.6:c.768C>T	ENSP00000477056.1:p.Pro256=
NM_000202.6:c.1401C>T	NP_000193.1:p.Pro467=
NM_001166550.2:c.1131C>T	NP_001160022.1:p.Pro377=
NM_000202.7:c.1401C>T	NP_000193.1:p.Pro467=
NM_001166550.3:c.1131C>T	NP_001160022.1:p.Pro377=
NM_000202.8:c.1401C>T MANE Select	NP_000193.1:p.Pro467=
NM_001166550.4:c.1131C>T	NP_001160022.1:p.Pro377=