Canonical Allele Identifier: CA1433068729
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002125G= , CM000666.2:g.1002125G= GRCh38
NC_000004.11:g.995913G= , CM000666.1:g.995913G= GRCh37
NC_000004.10:g.985913G= NCBI36
NG_008103.1:g.20129G=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.936G= ENSP00000247933.4:p.Trp312=
ENST00000514224.2:c.936G= MANE Select ENSP00000425081.2:p.Trp312=
ENST00000652070.1:n.992G=
ENST00000247933.8:c.936G= ENSP00000247933.4:p.Trp312=
ENST00000514224.1:c.540G= ENSP00000425081.1:p.Trp180=
ENST00000514698.5:n.936G=
NM_000203.4:c.936G= NP_000194.2:p.Trp312=
NR_110313.1:n.1024G=
XM_006713882.2:c.540G= XP_006713945.1:p.Trp180=
XM_011513459.1:c.895G= XP_011511761.1:p.Glu299=
XM_011513460.1:c.795G= XP_011511762.1:p.Trp265=
XM_011513461.1:c.729G= XP_011511763.1:p.Trp243=
XM_011513462.1:c.648G= XP_011511764.1:p.Trp216=
XM_011513463.1:c.648G= XP_011511765.1:p.Trp216=
XR_924947.1:n.1005G=
NM_000203.5:c.936G= MANE Select NP_000194.2:p.Trp312=
NM_001363576.1:c.540G= NP_001350505.1:p.Trp180=
XM_011513461.2:c.729G= XP_011511763.1:p.Trp243=
XM_017008163.1:c.-25G= XP_016863652.1:n.-25G=