Canonical Allele Identifier: CA2473585310
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45013781C= , CM000663.2:g.45013781C= GRCh38
NC_000001.10:g.45479453C= , CM000663.1:g.45479453C= GRCh37
NC_000001.9:g.45252040C= NCBI36
NG_007122.2:g.6624C=
NG_033058.1:g.2575G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246337.9:c.464C= MANE Select ENSP00000246337.4:p.Ala155=
ENST00000434478.6:c.518C= ENSP00000404489.2:p.Ala173=
ENST00000491773.6:c.359C= ENSP00000498551.1:p.Ala120=
ENST00000636293.1:c.464C= ENSP00000490710.1:p.Ala155=
ENST00000636836.1:c.464C= ENSP00000490594.1:p.Ala155=
ENST00000651476.1:c.359C= ENSP00000498668.1:p.Ala120=
ENST00000652165.1:c.359C= ENSP00000498295.1:p.Ala120=
ENST00000652287.1:c.401C= ENSP00000498413.1:p.Ala134=
ENST00000652514.1:c.425C= ENSP00000498635.1:n.425C=
ENST00000246337.8:c.464C= ENSP00000246337.4:p.Ala155=
ENST00000428106.1:c.444C=
ENST00000434478.5:c.401C= ENSP00000404489.1:p.Ala134=
ENST00000460334.5:n.491C=
ENST00000460906.5:n.481C=
ENST00000462688.5:n.591C=
ENST00000463092.5:n.860C=
ENST00000469548.5:n.660C=
ENST00000473012.1:n.511C=
ENST00000478467.5:n.467C=
ENST00000486699.5:n.584C=
ENST00000490385.5:n.538C=
ENST00000491300.5:n.583C=
ENST00000491773.5:n.618C=
ENST00000494399.5:n.604C=
ENST00000496439.1:n.443C=
NM_000374.4:c.464C= NP_000365.3:p.Ala155=
NR_036510.1:n.647C=
XM_005271169.1:c.248C= XP_005271226.1:p.Ala83=
XM_005271170.1:c.248C= XP_005271227.1:p.Ala83=
XM_011542080.1:c.401C= XP_011540382.1:p.Ala134=
XM_011542081.1:c.296C= XP_011540383.1:p.Ala99=
NM_000374.5:c.464C= MANE Select NP_000365.3:p.Ala155=
NR_158184.1:n.545C=
NR_158185.1:n.495C=
NR_036510.2:n.526C=