Canonical Allele Identifier: CA2473585497
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45013954A= , CM000663.2:g.45013954A= GRCh38
NC_000001.10:g.45479626A= , CM000663.1:g.45479626A= GRCh37
NC_000001.9:g.45252213A= NCBI36
NG_007122.2:g.6797A=
NG_033058.1:g.2402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246337.9:c.520A= MANE Select ENSP00000246337.4:p.Met174=
ENST00000434478.6:c.574A= ENSP00000404489.2:p.Met192=
ENST00000491773.6:c.415A= ENSP00000498551.1:p.Met139=
ENST00000636293.1:c.520A= ENSP00000490710.1:p.Met174=
ENST00000636836.1:c.520A= ENSP00000490594.1:p.Met174=
ENST00000651476.1:c.415A= ENSP00000498668.1:p.Met139=
ENST00000652165.1:c.415A= ENSP00000498295.1:p.Met139=
ENST00000652287.1:c.457A= ENSP00000498413.1:p.Met153=
ENST00000652514.1:c.481A= ENSP00000498635.1:n.481A=
ENST00000246337.8:c.520A= ENSP00000246337.4:p.Met174=
ENST00000428106.1:c.454+163A=
ENST00000434478.5:c.457A= ENSP00000404489.1:p.Met153=
ENST00000460334.5:n.547A=
ENST00000460906.5:n.654A=
ENST00000462688.5:n.647A=
ENST00000469548.5:n.716A=
ENST00000473012.1:n.567A=
ENST00000478467.5:n.523A=
ENST00000486699.5:n.640A=
ENST00000490385.5:n.594A=
ENST00000491300.5:n.639A=
ENST00000491773.5:n.674A=
ENST00000494399.5:n.660A=
ENST00000496439.1:n.616A=
NM_000374.4:c.520A= NP_000365.3:p.Met174=
NR_036510.1:n.703A=
XM_005271169.1:c.304A= XP_005271226.1:p.Met102=
XM_005271170.1:c.304A= XP_005271227.1:p.Met102=
XM_011542080.1:c.457A= XP_011540382.1:p.Met153=
XM_011542081.1:c.352A= XP_011540383.1:p.Met118=
NM_000374.5:c.520A= MANE Select NP_000365.3:p.Met174=
NR_158184.1:n.601A=
NR_158185.1:n.551A=
NR_036510.2:n.582A=