Canonical Allele Identifier: CA2465009253

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498275G= , CM000685.2:g.149498275G=	GRCh38
NC_000023.10:g.148579806G= , CM000685.1:g.148579806G=	GRCh37
NC_000023.9:g.148387711G=	NCBI36
NG_011900.3:g.12060C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.540C= MANE Select	ENSP00000339801.6:p.Ala180=
ENST00000651111.1:c.-94C=	ENSP00000498395.1:n.-94C=
ENST00000340855.10:c.540C=	ENSP00000339801.6:p.Ala180=
ENST00000370441.8:c.540C=	ENSP00000359470.4:p.Ala180=
ENST00000422081.6:c.-94C=	ENSP00000477056.1:n.-94C=
ENST00000441880.1:n.114-11177C=
ENST00000464251.5:c.466C=	ENSP00000428980.1:n.466C=
ENST00000466323.5:c.540C=	ENSP00000418264.1:p.Ala180=
ENST00000490775.5:n.325C=
ENST00000523759.5:n.654C=
NM_000202.6:c.540C=	NP_000193.1:p.Ala180=
NM_001166550.2:c.270C=	NP_001160022.1:p.Ala90=
NM_006123.4:c.540C=	NP_006114.1:p.Ala180=
NR_104128.1:n.757C=
NM_000202.7:c.540C=	NP_000193.1:p.Ala180=
NM_001166550.3:c.270C=	NP_001160022.1:p.Ala90=
NM_000202.8:c.540C= MANE Select	NP_000193.1:p.Ala180=
NM_001166550.4:c.270C=	NP_001160022.1:p.Ala90=
NM_006123.5:c.540C=	NP_006114.1:p.Ala180=
NR_104128.2:n.709C=