Canonical Allele Identifier: CA2465010884

Gene: IDS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149503432T= , CM000685.2:g.149503432T=	GRCh38
NC_000023.10:g.148584962T= , CM000685.1:g.148584962T=	GRCh37
NC_000023.9:g.148392867T=	NCBI36
NG_011900.3:g.6903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.298A= MANE Select	ENSP00000339801.6:p.Thr100=
ENST00000651111.1:c.-215-2395A=	ENSP00000498395.1:n.-215-2395A=
ENST00000340855.10:c.298A=	ENSP00000339801.6:p.Thr100=
ENST00000370441.8:c.298A=	ENSP00000359470.4:p.Thr100=
ENST00000422081.6:c.-215-2395A=	ENSP00000477056.1:n.-215-2395A=
ENST00000427113.2:n.770-1209A=
ENST00000428056.6:c.298A=	ENSP00000390241.2:p.Thr100=
ENST00000441880.1:n.114-16334A=
ENST00000464251.5:c.121A=	ENSP00000428980.1:p.Thr41=
ENST00000466323.5:c.298A=	ENSP00000418264.1:p.Thr100=
ENST00000523759.5:n.533-2395A=
NM_000202.6:c.298A=	NP_000193.1:p.Thr100=
NM_001166550.2:c.28A=	NP_001160022.1:p.Thr10=
NM_006123.4:c.298A=	NP_006114.1:p.Thr100=
NR_104128.1:n.515A=
NM_000202.7:c.298A=	NP_000193.1:p.Thr100=
NM_001166550.3:c.28A=	NP_001160022.1:p.Thr10=
NM_000202.8:c.298A= MANE Select	NP_000193.1:p.Thr100=
NM_001166550.4:c.28A=	NP_001160022.1:p.Thr10=
NM_006123.5:c.298A=	NP_006114.1:p.Thr100=
NR_104128.2:n.467A=