Canonical Allele Identifier: CA355961809

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.995337C>T (hg19) ; chr4:g.1001549C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1001549C>T , CM000666.2:g.1001549C>T	GRCh38
NC_000004.11:g.995337C>T , CM000666.1:g.995337C>T	GRCh37
NC_000004.10:g.985337C>T	NCBI36
NG_008103.1:g.19553C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.575C>T	ENSP00000247933.4:p.Ser192Phe
ENST00000514224.2:c.575C>T MANE Select	ENSP00000425081.2:p.Ser192Phe
ENST00000652070.1:n.631C>T
ENST00000247933.8:c.575C>T	ENSP00000247933.4:p.Ser192Phe
ENST00000502910.5:c.434C>T	ENSP00000422952.1:p.Ser145Phe
ENST00000504568.5:c.535C>T
ENST00000509948.5:c.368C>T	ENSP00000424227.1:p.Ser123Phe
ENST00000514192.5:c.392C>T	ENSP00000423685.1:p.Ser131Phe
ENST00000514224.1:c.179C>T	ENSP00000425081.1:p.Ser60Phe
ENST00000514698.5:n.475C>T
NM_000203.4:c.575C>T	NP_000194.2:p.Ser192Phe
NR_110313.1:n.663C>T
XM_006713882.2:c.179C>T	XP_006713945.1:p.Ser60Phe
XM_011513459.1:c.434C>T	XP_011511761.1:p.Ser145Phe
XM_011513460.1:c.434C>T	XP_011511762.1:p.Ser145Phe
XM_011513461.1:c.368C>T	XP_011511763.1:p.Ser123Phe
XM_011513462.1:c.287C>T	XP_011511764.1:p.Ser96Phe
XM_011513463.1:c.287C>T	XP_011511765.1:p.Ser96Phe
XR_924947.1:n.644C>T
NM_000203.5:c.575C>T MANE Select	NP_000194.2:p.Ser192Phe
NM_001363576.1:c.179C>T	NP_001350505.1:p.Ser60Phe
XM_011513461.2:c.368C>T	XP_011511763.1:p.Ser123Phe
XM_017008163.1:c.-414C>T	XP_016863652.1:n.-414C>T