Canonical Allele Identifier: CA2465006764

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490319T= , CM000685.2:g.149490319T=	GRCh38
NC_000023.10:g.148571850T= , CM000685.1:g.148571850T=	GRCh37
NC_000023.9:g.148379755T=	NCBI36
NG_011900.3:g.20016A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.1001A= MANE Select	ENSP00000339801.6:p.Asp334=
ENST00000651111.1:c.368A=	ENSP00000498395.1:p.Asp123=
ENST00000340855.10:c.1001A=	ENSP00000339801.6:p.Asp334=
ENST00000370441.8:c.1001A=	ENSP00000359470.4:p.Asp334=
ENST00000422081.6:c.368A=	ENSP00000477056.1:p.Asp123=
ENST00000441880.1:n.114-3221A=
ENST00000464251.5:c.927A=	ENSP00000428980.1:n.927A=
ENST00000466323.5:c.*192A=	ENSP00000418264.1:n.*192A=
ENST00000490775.5:n.786A=
NM_000202.6:c.1001A=	NP_000193.1:p.Asp334=
NM_001166550.2:c.731A=	NP_001160022.1:p.Asp244=
NM_006123.4:c.1001A=	NP_006114.1:p.Asp334=
NR_104128.1:n.1348A=
NM_000202.7:c.1001A=	NP_000193.1:p.Asp334=
NM_001166550.3:c.731A=	NP_001160022.1:p.Asp244=
NM_000202.8:c.1001A= MANE Select	NP_000193.1:p.Asp334=
NM_001166550.4:c.731A=	NP_001160022.1:p.Asp244=
NM_006123.5:c.1001A=	NP_006114.1:p.Asp334=
NR_104128.2:n.1300A=