Canonical Allele Identifier: CA2465006791

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490402A= , CM000685.2:g.149490402A=	GRCh38
NC_000023.10:g.148571933A= , CM000685.1:g.148571933A=	GRCh37
NC_000023.9:g.148379838A=	NCBI36
NG_011900.3:g.19933T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.918T= MANE Select	ENSP00000339801.6:p.Tyr306=
ENST00000651111.1:c.285T=	ENSP00000498395.1:p.Tyr95=
ENST00000340855.10:c.918T=	ENSP00000339801.6:p.Tyr306=
ENST00000370441.8:c.918T=	ENSP00000359470.4:p.Tyr306=
ENST00000422081.6:c.285T=	ENSP00000477056.1:p.Tyr95=
ENST00000441880.1:n.114-3304T=
ENST00000464251.5:c.844T=	ENSP00000428980.1:n.844T=
ENST00000466323.5:c.*109T=	ENSP00000418264.1:n.*109T=
ENST00000490775.5:n.703T=
NM_000202.6:c.918T=	NP_000193.1:p.Tyr306=
NM_001166550.2:c.648T=	NP_001160022.1:p.Tyr216=
NM_006123.4:c.918T=	NP_006114.1:p.Tyr306=
NR_104128.1:n.1265T=
NM_000202.7:c.918T=	NP_000193.1:p.Tyr306=
NM_001166550.3:c.648T=	NP_001160022.1:p.Tyr216=
NM_000202.8:c.918T= MANE Select	NP_000193.1:p.Tyr306=
NM_001166550.4:c.648T=	NP_001160022.1:p.Tyr216=
NM_006123.5:c.918T=	NP_006114.1:p.Tyr306=
NR_104128.2:n.1217T=