Canonical Allele Identifier: CA2694909269

Gene: IDS

Linked Data

• ClinVar Variation Id: 2998609
• ClinVar RCV Id: RCV003859256
• gnomAD v4: X-149490458-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490459del , CM000685.2:g.149490459del	GRCh38
NC_000023.10:g.148571990del , CM000685.1:g.148571990del	GRCh37
NC_000023.9:g.148379895del	NCBI36
NG_011900.3:g.19876del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.880-19del MANE Select	ENSP00000339801.6:n.880-19del
ENST00000651111.1:c.247-19del	ENSP00000498395.1:n.247-19del
ENST00000340855.10:c.880-19del	ENSP00000339801.6:n.880-19del
ENST00000370441.8:c.880-19del	ENSP00000359470.4:n.880-19del
ENST00000422081.6:c.247-19del	ENSP00000477056.1:n.247-19del
ENST00000441880.1:n.114-3361del
ENST00000464251.5:c.806-19del	ENSP00000428980.1:n.806-19del
ENST00000466323.5:c.*71-19del	ENSP00000418264.1:n.*71-19del
ENST00000490775.5:n.665-19del
NM_000202.6:c.880-19del	NP_000193.1:n.880-19del
NM_001166550.2:c.610-19del	NP_001160022.1:n.610-19del
NM_006123.4:c.880-19del	NP_006114.1:n.880-19del
NR_104128.1:n.1227-19del
NM_000202.7:c.880-19del	NP_000193.1:n.880-19del
NM_001166550.3:c.610-19del	NP_001160022.1:n.610-19del
NM_000202.8:c.880-19del MANE Select	NP_000193.1:n.880-19del
NM_001166550.4:c.610-19del	NP_001160022.1:n.610-19del
NM_006123.5:c.880-19del	NP_006114.1:n.880-19del
NR_104128.2:n.1179-19del