Canonical Allele Identifier: CA2465006802

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149490431G= , CM000685.2:g.149490431G=	GRCh38
NC_000023.10:g.148571962G= , CM000685.1:g.148571962G=	GRCh37
NC_000023.9:g.148379867G=	NCBI36
NG_011900.3:g.19904C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.889C= MANE Select	ENSP00000339801.6:p.Arg297=
ENST00000651111.1:c.256C=	ENSP00000498395.1:p.Arg86=
ENST00000340855.10:c.889C=	ENSP00000339801.6:p.Arg297=
ENST00000370441.8:c.889C=	ENSP00000359470.4:p.Arg297=
ENST00000422081.6:c.256C=	ENSP00000477056.1:p.Arg86=
ENST00000441880.1:n.114-3333C=
ENST00000464251.5:c.815C=	ENSP00000428980.1:n.815C=
ENST00000466323.5:c.*80C=	ENSP00000418264.1:n.*80C=
ENST00000490775.5:n.674C=
NM_000202.6:c.889C=	NP_000193.1:p.Arg297=
NM_001166550.2:c.619C=	NP_001160022.1:p.Arg207=
NM_006123.4:c.889C=	NP_006114.1:p.Arg297=
NR_104128.1:n.1236C=
NM_000202.7:c.889C=	NP_000193.1:p.Arg297=
NM_001166550.3:c.619C=	NP_001160022.1:p.Arg207=
NM_000202.8:c.889C= MANE Select	NP_000193.1:p.Arg297=
NM_001166550.4:c.619C=	NP_001160022.1:p.Arg207=
NM_006123.5:c.889C=	NP_006114.1:p.Arg297=
NR_104128.2:n.1188C=