Canonical Allele Identifier: CA2574350873
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45013866dup , CM000663.2:g.45013866dup GRCh38
NC_000001.10:g.45479538dup , CM000663.1:g.45479538dup GRCh37
NC_000001.9:g.45252125dup NCBI36
NG_007122.2:g.6709dup
NG_033058.1:g.2492dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000246337.9:c.475-43dup MANE Select ENSP00000246337.4:n.475-43dup
ENST00000434478.6:c.529-43dup ENSP00000404489.2:n.529-43dup
ENST00000491773.6:c.370-43dup ENSP00000498551.1:n.370-43dup
ENST00000636293.1:c.475-43dup ENSP00000490710.1:n.475-43dup
ENST00000636836.1:c.475-43dup ENSP00000490594.1:n.475-43dup
ENST00000651476.1:c.370-43dup ENSP00000498668.1:n.370-43dup
ENST00000652165.1:c.370-43dup ENSP00000498295.1:n.370-43dup
ENST00000652287.1:c.412-43dup ENSP00000498413.1:n.412-43dup
ENST00000652514.1:c.436-43dup ENSP00000498635.1:n.436-43dup
ENST00000246337.8:c.475-43dup ENSP00000246337.4:n.475-43dup
ENST00000428106.1:c.454+75dup
ENST00000434478.5:c.412-43dup ENSP00000404489.1:n.412-43dup
ENST00000460334.5:n.502-43dup
ENST00000460906.5:n.566dup
ENST00000462688.5:n.602-43dup
ENST00000463092.5:n.945dup
ENST00000469548.5:n.671-43dup
ENST00000473012.1:n.522-43dup
ENST00000478467.5:n.478-43dup
ENST00000486699.5:n.595-43dup
ENST00000490385.5:n.549-43dup
ENST00000491300.5:n.594-43dup
ENST00000491773.5:n.629-43dup
ENST00000494399.5:n.615-43dup
ENST00000496439.1:n.528dup
NM_000374.4:c.475-43dup NP_000365.3:n.475-43dup
NR_036510.1:n.658-43dup
XM_005271169.1:c.259-43dup XP_005271226.1:n.259-43dup
XM_005271170.1:c.259-43dup XP_005271227.1:n.259-43dup
XM_011542080.1:c.412-43dup XP_011540382.1:n.412-43dup
XM_011542081.1:c.307-43dup XP_011540383.1:n.307-43dup
NM_000374.5:c.475-43dup MANE Select NP_000365.3:n.475-43dup
NR_158184.1:n.556-43dup
NR_158185.1:n.506-43dup
NR_036510.2:n.537-43dup