Canonical Allele Identifier: CA645068953

Gene: IDS

Linked Data

• dbSNP Id: rs1210033707
• gnomAD v2: X-148572062-A-G
• gnomAD v3: X-149490531-A-G
• gnomAD v4: X-149490531-A-G
• MyVariant Identifiers: chrX:g.148572062A>G (hg19) ; chrX:g.149490531A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490531A>G , CM000685.2:g.149490531A>G	GRCh38
NC_000023.10:g.148572062A>G , CM000685.1:g.148572062A>G	GRCh37
NC_000023.9:g.148379967A>G	NCBI36
NG_011900.3:g.19804T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-91T>C MANE Select	ENSP00000339801.6:n.880-91T>C
ENST00000651111.1:c.247-91T>C	ENSP00000498395.1:n.247-91T>C
ENST00000340855.10:c.880-91T>C	ENSP00000339801.6:n.880-91T>C
ENST00000370441.8:c.880-91T>C	ENSP00000359470.4:n.880-91T>C
ENST00000422081.6:c.247-91T>C	ENSP00000477056.1:n.247-91T>C
ENST00000441880.1:n.114-3433T>C
ENST00000464251.5:c.806-91T>C	ENSP00000428980.1:n.806-91T>C
ENST00000466323.5:c.*71-91T>C	ENSP00000418264.1:n.*71-91T>C
ENST00000490775.5:n.665-91T>C
NM_000202.6:c.880-91T>C	NP_000193.1:n.880-91T>C
NM_001166550.2:c.610-91T>C	NP_001160022.1:n.610-91T>C
NM_006123.4:c.880-91T>C	NP_006114.1:n.880-91T>C
NR_104128.1:n.1227-91T>C
NM_000202.7:c.880-91T>C	NP_000193.1:n.880-91T>C
NM_001166550.3:c.610-91T>C	NP_001160022.1:n.610-91T>C
NM_000202.8:c.880-91T>C MANE Select	NP_000193.1:n.880-91T>C
NM_001166550.4:c.610-91T>C	NP_001160022.1:n.610-91T>C
NM_006123.5:c.880-91T>C	NP_006114.1:n.880-91T>C
NR_104128.2:n.1179-91T>C