Canonical Allele Identifier: CA2465011147

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149504201G= , CM000685.2:g.149504201G=	GRCh38
NC_000023.10:g.148585731G= , CM000685.1:g.148585731G=	GRCh37
NC_000023.9:g.148393635G=	NCBI36
NG_011900.3:g.6134C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.196C= MANE Select	ENSP00000339801.6:p.Gln66=
ENST00000651111.1:c.-215-3164C=	ENSP00000498395.1:n.-215-3164C=
ENST00000340855.10:c.196C=	ENSP00000339801.6:p.Gln66=
ENST00000370441.8:c.196C=	ENSP00000359470.4:p.Gln66=
ENST00000422081.6:c.-215-3164C=	ENSP00000477056.1:n.-215-3164C=
ENST00000427113.2:n.770-1978C=
ENST00000428056.6:c.196C=	ENSP00000390241.2:p.Gln66=
ENST00000441880.1:n.114-17103C=
ENST00000464251.5:c.19C=	ENSP00000428980.1:p.Gln7=
ENST00000466323.5:c.196C=	ENSP00000418264.1:p.Gln66=
ENST00000521702.1:c.196C=	ENSP00000429745.1:p.Gln66=
ENST00000523759.5:n.533-3164C=
NM_000202.6:c.196C=	NP_000193.1:p.Gln66=
NM_001166550.2:c.-31C=	NP_001160022.1:n.-31C=
NM_006123.4:c.196C=	NP_006114.1:p.Gln66=
NR_104128.1:n.413C=
NM_000202.7:c.196C=	NP_000193.1:p.Gln66=
NM_001166550.3:c.-31C=	NP_001160022.1:n.-31C=
NM_000202.8:c.196C= MANE Select	NP_000193.1:p.Gln66=
NM_001166550.4:c.-31C=	NP_001160022.1:n.-31C=
NM_006123.5:c.196C=	NP_006114.1:p.Gln66=
NR_104128.2:n.365C=