Canonical Allele Identifier: CA519057538

Gene: IDS

Linked Data

• MyVariant Identifiers: chrX:g.148568472T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149486941T>A , CM000685.2:g.149486941T>A	GRCh38
NC_000023.10:g.148568472T>A , CM000685.1:g.148568472T>A	GRCh37
NC_000023.9:g.148376377T>A	NCBI36
NG_011900.3:g.23394A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1164A>T MANE Select	ENSP00000339801.6:p.Ser388=
ENST00000651111.1:c.531A>T	ENSP00000498395.1:p.Ser177=
ENST00000340855.10:c.1164A>T	ENSP00000339801.6:p.Ser388=
ENST00000422081.6:c.531A>T	ENSP00000477056.1:p.Ser177=
ENST00000441880.1:n.271A>T
NM_000202.6:c.1164A>T	NP_000193.1:p.Ser388=
NM_001166550.2:c.894A>T	NP_001160022.1:p.Ser298=
NM_000202.7:c.1164A>T	NP_000193.1:p.Ser388=
NM_001166550.3:c.894A>T	NP_001160022.1:p.Ser298=
NM_000202.8:c.1164A>T MANE Select	NP_000193.1:p.Ser388=
NM_001166550.4:c.894A>T	NP_001160022.1:p.Ser298=