Canonical Allele Identifier: CA355963519
Gene: IDUA HGNC NCBI

Linked Data

gnomAD v4: 4-1002734-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002734G>A , CM000666.2:g.1002734G>A GRCh38
NC_000004.11:g.996522G>A , CM000666.1:g.996522G>A GRCh37
NC_000004.10:g.986522G>A NCBI36
NG_008103.1:g.20738G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1192G>A ENSP00000247933.4:p.Glu398Lys
ENST00000514224.2:c.1192G>A MANE Select ENSP00000425081.2:p.Glu398Lys
ENST00000652070.1:n.1248G>A
ENST00000247933.8:c.1192G>A ENSP00000247933.4:p.Glu398Lys
ENST00000514224.1:c.796G>A ENSP00000425081.1:p.Glu266Lys
ENST00000514698.5:n.1299G>A
NM_000203.4:c.1192G>A NP_000194.2:p.Glu398Lys
NR_110313.1:n.1280G>A
XM_006713882.2:c.796G>A XP_006713945.1:p.Glu266Lys
XM_011513459.1:c.1258G>A XP_011511761.1:p.Glu420Lys
XM_011513460.1:c.1051G>A XP_011511762.1:p.Glu351Lys
XM_011513461.1:c.985G>A XP_011511763.1:p.Glu329Lys
XM_011513462.1:c.904G>A XP_011511764.1:p.Glu302Lys
XM_011513463.1:c.904G>A XP_011511765.1:p.Glu302Lys
XR_924947.1:n.1261G>A
NM_000203.5:c.1192G>A MANE Select NP_000194.2:p.Glu398Lys
NM_001363576.1:c.796G>A NP_001350505.1:p.Glu266Lys
XM_011513461.2:c.985G>A XP_011511763.1:p.Glu329Lys
XM_017008163.1:c.232G>A XP_016863652.1:p.Glu78Lys