Canonical Allele Identifier: CA519173973

Gene: IDS

Linked Data

• ClinVar Variation Id: 2732511
• ClinVar RCV Id: RCV003511410
• dbSNP Id: rs2089306640
• MyVariant Identifiers: chrX:g.148564595A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483064A>G , CM000685.2:g.149483064A>G	GRCh38
NC_000023.10:g.148564595A>G , CM000685.1:g.148564595A>G	GRCh37
NC_000023.9:g.148372500A>G	NCBI36
NG_011900.3:g.27271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1335T>C MANE Select	ENSP00000339801.6:p.Arg445=
ENST00000651111.1:c.702T>C	ENSP00000498395.1:p.Arg234=
ENST00000340855.10:c.1335T>C	ENSP00000339801.6:p.Arg445=
ENST00000422081.6:c.702T>C	ENSP00000477056.1:p.Arg234=
NM_000202.6:c.1335T>C	NP_000193.1:p.Arg445=
NM_001166550.2:c.1065T>C	NP_001160022.1:p.Arg355=
NM_000202.7:c.1335T>C	NP_000193.1:p.Arg445=
NM_001166550.3:c.1065T>C	NP_001160022.1:p.Arg355=
NM_000202.8:c.1335T>C MANE Select	NP_000193.1:p.Arg445=
NM_001166550.4:c.1065T>C	NP_001160022.1:p.Arg355=