Canonical Allele Identifier: CA2465009255

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149498298C= , CM000685.2:g.149498298C=	GRCh38
NC_000023.10:g.148579829C= , CM000685.1:g.148579829C=	GRCh37
NC_000023.9:g.148387734C=	NCBI36
NG_011900.3:g.12037G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.517G= MANE Select	ENSP00000339801.6:p.Gly173=
ENST00000651111.1:c.-117G=	ENSP00000498395.1:n.-117G=
ENST00000340855.10:c.517G=	ENSP00000339801.6:p.Gly173=
ENST00000370441.8:c.517G=	ENSP00000359470.4:p.Gly173=
ENST00000422081.6:c.-117G=	ENSP00000477056.1:n.-117G=
ENST00000441880.1:n.114-11200G=
ENST00000464251.5:c.443G=	ENSP00000428980.1:n.443G=
ENST00000466323.5:c.517G=	ENSP00000418264.1:p.Gly173=
ENST00000490775.5:n.302G=
ENST00000523759.5:n.631G=
NM_000202.6:c.517G=	NP_000193.1:p.Gly173=
NM_001166550.2:c.247G=	NP_001160022.1:p.Gly83=
NM_006123.4:c.517G=	NP_006114.1:p.Gly173=
NR_104128.1:n.734G=
NM_000202.7:c.517G=	NP_000193.1:p.Gly173=
NM_001166550.3:c.247G=	NP_001160022.1:p.Gly83=
NM_000202.8:c.517G= MANE Select	NP_000193.1:p.Gly173=
NM_001166550.4:c.247G=	NP_001160022.1:p.Gly83=
NM_006123.5:c.517G=	NP_006114.1:p.Gly173=
NR_104128.2:n.686G=