Canonical Allele Identifier: CA2465006793

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490410_149490412delinsCAG , CM000685.2:g.149490410_149490412delinsCAG	GRCh38
NC_000023.10:g.148571941_148571943delinsCAG , CM000685.1:g.148571941_148571943delinsCAG	GRCh37
NC_000023.9:g.148379846_148379848delinsCAG	NCBI36
NG_011900.3:g.19923_19925delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.908_910delinsCTG MANE Select	ENSP00000339801.6:p.Ser303=
ENST00000651111.1:c.275_277delinsCTG	ENSP00000498395.1:p.Ser92=
ENST00000340855.10:c.908_910delinsCTG	ENSP00000339801.6:p.Ser303=
ENST00000370441.8:c.908_910delinsCTG	ENSP00000359470.4:p.Ser303=
ENST00000422081.6:c.275_277delinsCTG	ENSP00000477056.1:p.Ser92=
ENST00000441880.1:n.114-3314_114-3312delinsCTG
ENST00000464251.5:c.834_836delinsCTG	ENSP00000428980.1:n.834_836delinsCTG
ENST00000466323.5:c.*99_*101delinsCTG	ENSP00000418264.1:n.*99_*101delinsCTG
ENST00000490775.5:n.693_695delinsCTG
NM_000202.6:c.908_910delinsCTG	NP_000193.1:p.Ser303=
NM_001166550.2:c.638_640delinsCTG	NP_001160022.1:p.Ser213=
NM_006123.4:c.908_910delinsCTG	NP_006114.1:p.Ser303=
NR_104128.1:n.1255_1257delinsCTG
NM_000202.7:c.908_910delinsCTG	NP_000193.1:p.Ser303=
NM_001166550.3:c.638_640delinsCTG	NP_001160022.1:p.Ser213=
NM_000202.8:c.908_910delinsCTG MANE Select	NP_000193.1:p.Ser303=
NM_001166550.4:c.638_640delinsCTG	NP_001160022.1:p.Ser213=
NM_006123.5:c.908_910delinsCTG	NP_006114.1:p.Ser303=
NR_104128.2:n.1207_1209delinsCTG