Canonical Allele Identifier: CA1433068737
Gene: IDUA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.1002128G= , CM000666.2:g.1002128G= GRCh38
NC_000004.11:g.995916G= , CM000666.1:g.995916G= GRCh37
NC_000004.10:g.985916G= NCBI36
NG_008103.1:g.20132G=

Transcript Alleles

HGVS Amino-acid change
ENST00000247933.9:c.939G= ENSP00000247933.4:p.Arg313=
ENST00000514224.2:c.939G= MANE Select ENSP00000425081.2:p.Arg313=
ENST00000652070.1:n.995G=
ENST00000247933.8:c.939G= ENSP00000247933.4:p.Arg313=
ENST00000514224.1:c.543G= ENSP00000425081.1:p.Arg181=
ENST00000514698.5:n.939G=
NM_000203.4:c.939G= NP_000194.2:p.Arg313=
NR_110313.1:n.1027G=
XM_006713882.2:c.543G= XP_006713945.1:p.Arg181=
XM_011513459.1:c.898G= XP_011511761.1:p.Gly300=
XM_011513460.1:c.798G= XP_011511762.1:p.Arg266=
XM_011513461.1:c.732G= XP_011511763.1:p.Arg244=
XM_011513462.1:c.651G= XP_011511764.1:p.Arg217=
XM_011513463.1:c.651G= XP_011511765.1:p.Arg217=
XR_924947.1:n.1008G=
NM_000203.5:c.939G= MANE Select NP_000194.2:p.Arg313=
NM_001363576.1:c.543G= NP_001350505.1:p.Arg181=
XM_011513461.2:c.732G= XP_011511763.1:p.Arg244=
XM_017008163.1:c.-22G= XP_016863652.1:n.-22G=