Canonical Allele Identifier: CA355965260
Gene: IDUA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1003609G>T , CM000666.2:g.1003609G>T GRCh38
NC_000004.11:g.997397G>T , CM000666.1:g.997397G>T GRCh37
NC_000004.10:g.987397G>T NCBI36
NG_008103.1:g.21613G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000247933.9:c.1711G>T ENSP00000247933.4:p.Glu571Ter
ENST00000514224.2:c.1711G>T MANE Select ENSP00000425081.2:p.Glu571Ter
ENST00000652070.1:n.1767G>T
ENST00000247933.8:c.1711G>T ENSP00000247933.4:p.Glu571Ter
ENST00000514224.1:c.1315G>T ENSP00000425081.1:p.Glu439Ter
ENST00000514417.1:n.103G>T
ENST00000514698.5:n.1818G>T
NM_000203.4:c.1711G>T NP_000194.2:p.Glu571Ter
NR_110313.1:n.1799G>T
XM_006713882.2:c.1315G>T XP_006713945.1:p.Glu439Ter
XM_011513459.1:c.1777G>T XP_011511761.1:p.Glu593Ter
XM_011513460.1:c.1570G>T XP_011511762.1:p.Glu524Ter
XM_011513461.1:c.1504G>T XP_011511763.1:p.Glu502Ter
XM_011513462.1:c.1423G>T XP_011511764.1:p.Glu475Ter
XM_011513463.1:c.1423G>T XP_011511765.1:p.Glu475Ter
XR_924947.1:n.1967G>T
NM_000203.5:c.1711G>T MANE Select NP_000194.2:p.Glu571Ter
NM_001363576.1:c.1315G>T NP_001350505.1:p.Glu439Ter
XM_011513461.2:c.1504G>T XP_011511763.1:p.Glu502Ter
XM_017008163.1:c.751G>T XP_016863652.1:p.Glu251Ter