Canonical Allele Identifier: CA645068983

Gene: IDS

Linked Data

• gnomAD v2: X-148572258-T-TC
• gnomAD v3: X-149490727-T-TC
• gnomAD v4: X-149490727-T-TC
• MyVariant Identifiers: chrX:g.148572258_148572259insC (hg19) ; chrX:g.149490727_149490728insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490727_149490728insC , CM000685.2:g.149490727_149490728insC	GRCh38
NC_000023.10:g.148572258_148572259insC , CM000685.1:g.148572258_148572259insC	GRCh37
NC_000023.9:g.148380163_148380164insC	NCBI36
NG_011900.3:g.19607_19608insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-288_880-287insG MANE Select	ENSP00000339801.6:n.880-288_880-287insG
ENST00000651111.1:c.247-288_247-287insG	ENSP00000498395.1:n.247-288_247-287insG
ENST00000340855.10:c.880-288_880-287insG	ENSP00000339801.6:n.880-288_880-287insG
ENST00000370441.8:c.880-288_880-287insG	ENSP00000359470.4:n.880-288_880-287insG
ENST00000422081.6:c.247-288_247-287insG	ENSP00000477056.1:n.247-288_247-287insG
ENST00000441880.1:n.114-3630_114-3629insG
ENST00000464251.5:c.806-288_806-287insG	ENSP00000428980.1:n.806-288_806-287insG
ENST00000466323.5:c.*71-288_*71-287insG	ENSP00000418264.1:n.*71-288_*71-287insG
ENST00000490775.5:n.665-288_665-287insG
NM_000202.6:c.880-288_880-287insG	NP_000193.1:n.880-288_880-287insG
NM_001166550.2:c.610-288_610-287insG	NP_001160022.1:n.610-288_610-287insG
NM_006123.4:c.880-288_880-287insG	NP_006114.1:n.880-288_880-287insG
NR_104128.1:n.1227-288_1227-287insG
NM_000202.7:c.880-288_880-287insG	NP_000193.1:n.880-288_880-287insG
NM_001166550.3:c.610-288_610-287insG	NP_001160022.1:n.610-288_610-287insG
NM_000202.8:c.880-288_880-287insG MANE Select	NP_000193.1:n.880-288_880-287insG
NM_001166550.4:c.610-288_610-287insG	NP_001160022.1:n.610-288_610-287insG
NM_006123.5:c.880-288_880-287insG	NP_006114.1:n.880-288_880-287insG
NR_104128.2:n.1179-288_1179-287insG