Canonical Allele Identifier: CA2465009209

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498145C= , CM000685.2:g.149498145C=	GRCh38
NC_000023.10:g.148579676C= , CM000685.1:g.148579676C=	GRCh37
NC_000023.9:g.148387581C=	NCBI36
NG_011900.3:g.12190G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.670G= MANE Select	ENSP00000339801.6:p.Gly224=
ENST00000651111.1:c.37G=	ENSP00000498395.1:p.Gly13=
ENST00000340855.10:c.670G=	ENSP00000339801.6:p.Gly224=
ENST00000370441.8:c.670G=	ENSP00000359470.4:p.Gly224=
ENST00000422081.6:c.37G=	ENSP00000477056.1:p.Gly13=
ENST00000441880.1:n.114-11047G=
ENST00000464251.5:c.596G=	ENSP00000428980.1:n.596G=
ENST00000466019.1:n.122G=
ENST00000466323.5:c.670G=	ENSP00000418264.1:p.Gly224=
ENST00000490775.5:n.455G=
NM_000202.6:c.670G=	NP_000193.1:p.Gly224=
NM_001166550.2:c.400G=	NP_001160022.1:p.Gly134=
NM_006123.4:c.670G=	NP_006114.1:p.Gly224=
NR_104128.1:n.887G=
NM_000202.7:c.670G=	NP_000193.1:p.Gly224=
NM_001166550.3:c.400G=	NP_001160022.1:p.Gly134=
NM_000202.8:c.670G= MANE Select	NP_000193.1:p.Gly224=
NM_001166550.4:c.400G=	NP_001160022.1:p.Gly134=
NM_006123.5:c.670G=	NP_006114.1:p.Gly224=
NR_104128.2:n.839G=