Canonical Allele Identifier: CA872891215

Gene: IDS

Linked Data

• dbSNP Id: rs1162308211
• gnomAD v3: X-149496723-G-A
• gnomAD v4: X-149496723-G-A
• MyVariant Identifiers: chrX:g.149496723G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149496723G>A , CM000685.2:g.149496723G>A	GRCh38
NC_000023.10:g.148578254G>A , CM000685.1:g.148578254G>A	GRCh37
NC_000023.9:g.148386159G>A	NCBI36
NG_011900.3:g.13612C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.709-207C>T MANE Select	ENSP00000339801.6:n.709-207C>T
ENST00000651111.1:c.76-207C>T	ENSP00000498395.1:n.76-207C>T
ENST00000340855.10:c.709-207C>T	ENSP00000339801.6:n.709-207C>T
ENST00000370441.8:c.709-207C>T	ENSP00000359470.4:n.709-207C>T
ENST00000422081.6:c.76-207C>T	ENSP00000477056.1:n.76-207C>T
ENST00000441880.1:n.114-9625C>T
ENST00000464251.5:c.635-207C>T	ENSP00000428980.1:n.635-207C>T
ENST00000466019.1:n.161-207C>T
ENST00000466323.5:c.709-207C>T	ENSP00000418264.1:n.709-207C>T
ENST00000490775.5:n.494-207C>T
NM_000202.6:c.709-207C>T	NP_000193.1:n.709-207C>T
NM_001166550.2:c.439-207C>T	NP_001160022.1:n.439-207C>T
NM_006123.4:c.709-207C>T	NP_006114.1:n.709-207C>T
NR_104128.1:n.926-207C>T
NM_000202.7:c.709-207C>T	NP_000193.1:n.709-207C>T
NM_001166550.3:c.439-207C>T	NP_001160022.1:n.439-207C>T
NM_000202.8:c.709-207C>T MANE Select	NP_000193.1:n.709-207C>T
NM_001166550.4:c.439-207C>T	NP_001160022.1:n.439-207C>T
NM_006123.5:c.709-207C>T	NP_006114.1:n.709-207C>T
NR_104128.2:n.878-207C>T