Canonical Allele Identifier: CA519173915

Gene: IDS

Linked Data

• gnomAD v4: X-149483022-T-C
• MyVariant Identifiers: chrX:g.148564553T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149483022T>C , CM000685.2:g.149483022T>C	GRCh38
NC_000023.10:g.148564553T>C , CM000685.1:g.148564553T>C	GRCh37
NC_000023.9:g.148372458T>C	NCBI36
NG_011900.3:g.27313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1377A>G MANE Select	ENSP00000339801.6:p.Glu459=
ENST00000651111.1:c.744A>G	ENSP00000498395.1:p.Glu248=
ENST00000340855.10:c.1377A>G	ENSP00000339801.6:p.Glu459=
ENST00000422081.6:c.744A>G	ENSP00000477056.1:p.Glu248=
NM_000202.6:c.1377A>G	NP_000193.1:p.Glu459=
NM_001166550.2:c.1107A>G	NP_001160022.1:p.Glu369=
NM_000202.7:c.1377A>G	NP_000193.1:p.Glu459=
NM_001166550.3:c.1107A>G	NP_001160022.1:p.Glu369=
NM_000202.8:c.1377A>G MANE Select	NP_000193.1:p.Glu459=
NM_001166550.4:c.1107A>G	NP_001160022.1:p.Glu369=