Canonical Allele Identifier: CA350641

Gene: IDS

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.149504206A>T , CM000685.2:g.149504206A>T	GRCh38
NC_000023.10:g.148585736A>T , CM000685.1:g.148585736A>T	GRCh37
NC_000023.9:g.148393640A>T	NCBI36
NG_011900.3:g.6129T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340855.11:c.191T>A MANE Select	ENSP00000339801.6:p.Ile64Asn
ENST00000651111.1:c.-215-3169T>A	ENSP00000498395.1:n.-215-3169T>A
ENST00000340855.10:c.191T>A	ENSP00000339801.6:p.Ile64Asn
ENST00000370441.8:c.191T>A	ENSP00000359470.4:p.Ile64Asn
ENST00000422081.6:c.-215-3169T>A	ENSP00000477056.1:n.-215-3169T>A
ENST00000427113.2:n.770-1983T>A
ENST00000428056.6:c.191T>A	ENSP00000390241.2:p.Ile64Asn
ENST00000441880.1:n.114-17108T>A
ENST00000464251.5:c.14T>A	ENSP00000428980.1:p.Ile5Asn
ENST00000466323.5:c.191T>A	ENSP00000418264.1:p.Ile64Asn
ENST00000521702.1:c.191T>A	ENSP00000429745.1:p.Ile64Asn
ENST00000523759.5:n.533-3169T>A
NM_000202.6:c.191T>A	NP_000193.1:p.Ile64Asn
NM_001166550.2:c.-36T>A	NP_001160022.1:n.-36T>A
NM_006123.4:c.191T>A	NP_006114.1:p.Ile64Asn
NR_104128.1:n.408T>A
NM_000202.7:c.191T>A	NP_000193.1:p.Ile64Asn
NM_001166550.3:c.-36T>A	NP_001160022.1:n.-36T>A
NM_000202.8:c.191T>A MANE Select	NP_000193.1:p.Ile64Asn
NM_001166550.4:c.-36T>A	NP_001160022.1:n.-36T>A
NM_006123.5:c.191T>A	NP_006114.1:p.Ile64Asn
NR_104128.2:n.360T>A