Canonical Allele Identifier: CA355965263

Gene: IDUA

Linked Data

• MyVariant Identifiers: chr4:g.997398A>T (hg19) ; chr4:g.1003610A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1003610A>T , CM000666.2:g.1003610A>T	GRCh38
NC_000004.11:g.997398A>T , CM000666.1:g.997398A>T	GRCh37
NC_000004.10:g.987398A>T	NCBI36
NG_008103.1:g.21614A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247933.9:c.1712A>T	ENSP00000247933.4:p.Glu571Val
ENST00000514224.2:c.1712A>T MANE Select	ENSP00000425081.2:p.Glu571Val
ENST00000652070.1:n.1768A>T
ENST00000247933.8:c.1712A>T	ENSP00000247933.4:p.Glu571Val
ENST00000514224.1:c.1316A>T	ENSP00000425081.1:p.Glu439Val
ENST00000514417.1:n.104A>T
ENST00000514698.5:n.1819A>T
NM_000203.4:c.1712A>T	NP_000194.2:p.Glu571Val
NR_110313.1:n.1800A>T
XM_006713882.2:c.1316A>T	XP_006713945.1:p.Glu439Val
XM_011513459.1:c.1778A>T	XP_011511761.1:p.Glu593Val
XM_011513460.1:c.1571A>T	XP_011511762.1:p.Glu524Val
XM_011513461.1:c.1505A>T	XP_011511763.1:p.Glu502Val
XM_011513462.1:c.1424A>T	XP_011511764.1:p.Glu475Val
XM_011513463.1:c.1424A>T	XP_011511765.1:p.Glu475Val
XR_924947.1:n.1968A>T
NM_000203.5:c.1712A>T MANE Select	NP_000194.2:p.Glu571Val
NM_001363576.1:c.1316A>T	NP_001350505.1:p.Glu439Val
XM_011513461.2:c.1505A>T	XP_011511763.1:p.Glu502Val
XM_017008163.1:c.752A>T	XP_016863652.1:p.Glu251Val