Canonical Allele Identifier: CA2473585323
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45013788C= , CM000663.2:g.45013788C= GRCh38
NC_000001.10:g.45479460C= , CM000663.1:g.45479460C= GRCh37
NC_000001.9:g.45252047C= NCBI36
NG_007122.2:g.6631C=
NG_033058.1:g.2568G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246337.9:c.471C= MANE Select ENSP00000246337.4:p.Ala157=
ENST00000434478.6:c.525C= ENSP00000404489.2:p.Ala175=
ENST00000491773.6:c.366C= ENSP00000498551.1:p.Ala122=
ENST00000636293.1:c.471C= ENSP00000490710.1:p.Ala157=
ENST00000636836.1:c.471C= ENSP00000490594.1:p.Ala157=
ENST00000651476.1:c.366C= ENSP00000498668.1:p.Ala122=
ENST00000652165.1:c.366C= ENSP00000498295.1:p.Ala122=
ENST00000652287.1:c.408C= ENSP00000498413.1:p.Ala136=
ENST00000652514.1:c.432C= ENSP00000498635.1:n.432C=
ENST00000246337.8:c.471C= ENSP00000246337.4:p.Ala157=
ENST00000428106.1:c.451C=
ENST00000434478.5:c.408C= ENSP00000404489.1:p.Ala136=
ENST00000460334.5:n.498C=
ENST00000460906.5:n.488C=
ENST00000462688.5:n.598C=
ENST00000463092.5:n.867C=
ENST00000469548.5:n.667C=
ENST00000473012.1:n.518C=
ENST00000478467.5:n.474C=
ENST00000486699.5:n.591C=
ENST00000490385.5:n.545C=
ENST00000491300.5:n.590C=
ENST00000491773.5:n.625C=
ENST00000494399.5:n.611C=
ENST00000496439.1:n.450C=
NM_000374.4:c.471C= NP_000365.3:p.Ala157=
NR_036510.1:n.654C=
XM_005271169.1:c.255C= XP_005271226.1:p.Ala85=
XM_005271170.1:c.255C= XP_005271227.1:p.Ala85=
XM_011542080.1:c.408C= XP_011540382.1:p.Ala136=
XM_011542081.1:c.303C= XP_011540383.1:p.Ala101=
NM_000374.5:c.471C= MANE Select NP_000365.3:p.Ala157=
NR_158184.1:n.552C=
NR_158185.1:n.502C=
NR_036510.2:n.533C=