Canonical Allele Identifier: CA2473585426
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45013874G= , CM000663.2:g.45013874G= GRCh38
NC_000001.10:g.45479546G= , CM000663.1:g.45479546G= GRCh37
NC_000001.9:g.45252133G= NCBI36
NG_007122.2:g.6717G=
NG_033058.1:g.2482C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246337.9:c.475-35G= MANE Select ENSP00000246337.4:n.475-35G=
ENST00000434478.6:c.529-35G= ENSP00000404489.2:n.529-35G=
ENST00000491773.6:c.370-35G= ENSP00000498551.1:n.370-35G=
ENST00000636293.1:c.475-35G= ENSP00000490710.1:n.475-35G=
ENST00000636836.1:c.475-35G= ENSP00000490594.1:n.475-35G=
ENST00000651476.1:c.370-35G= ENSP00000498668.1:n.370-35G=
ENST00000652165.1:c.370-35G= ENSP00000498295.1:n.370-35G=
ENST00000652287.1:c.412-35G= ENSP00000498413.1:n.412-35G=
ENST00000652514.1:c.436-35G= ENSP00000498635.1:n.436-35G=
ENST00000246337.8:c.475-35G= ENSP00000246337.4:n.475-35G=
ENST00000428106.1:c.454+83G=
ENST00000434478.5:c.412-35G= ENSP00000404489.1:n.412-35G=
ENST00000460334.5:n.502-35G=
ENST00000460906.5:n.574G=
ENST00000462688.5:n.602-35G=
ENST00000463092.5:n.953G=
ENST00000469548.5:n.671-35G=
ENST00000473012.1:n.522-35G=
ENST00000478467.5:n.478-35G=
ENST00000486699.5:n.595-35G=
ENST00000490385.5:n.549-35G=
ENST00000491300.5:n.594-35G=
ENST00000491773.5:n.629-35G=
ENST00000494399.5:n.615-35G=
ENST00000496439.1:n.536G=
NM_000374.4:c.475-35G= NP_000365.3:n.475-35G=
NR_036510.1:n.658-35G=
XM_005271169.1:c.259-35G= XP_005271226.1:n.259-35G=
XM_005271170.1:c.259-35G= XP_005271227.1:n.259-35G=
XM_011542080.1:c.412-35G= XP_011540382.1:n.412-35G=
XM_011542081.1:c.307-35G= XP_011540383.1:n.307-35G=
NM_000374.5:c.475-35G= MANE Select NP_000365.3:n.475-35G=
NR_158184.1:n.556-35G=
NR_158185.1:n.506-35G=
NR_036510.2:n.537-35G=