Canonical Allele Identifier: CA2473585860
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45015401A= , CM000663.2:g.45015401A= GRCh38
NC_000001.10:g.45481073A= , CM000663.1:g.45481073A= GRCh37
NC_000001.9:g.45253660A= NCBI36
NG_007122.2:g.8244A=
NG_033058.1:g.955T=

Transcript Alleles

HGVS Amino-acid change
ENST00000246337.9:c.1007A= MANE Select ENSP00000246337.4:p.Asn336=
ENST00000491773.6:c.764A= ENSP00000498551.1:p.Asn255=
ENST00000636293.1:c.869A= ENSP00000490710.1:p.Asn290=
ENST00000636836.1:c.*43A= ENSP00000490594.1:n.*43A=
ENST00000651476.1:c.902A= ENSP00000498668.1:p.Asn301=
ENST00000652165.1:c.764A= ENSP00000498295.1:p.Asn255=
ENST00000652287.1:c.944A= ENSP00000498413.1:p.Asn315=
ENST00000652514.1:c.968A= ENSP00000498635.1:n.968A=
ENST00000246337.8:c.1007A= ENSP00000246337.4:p.Asn336=
ENST00000465678.1:n.752A=
ENST00000472254.1:n.760A=
ENST00000494399.5:n.1674A=
NM_000374.4:c.1007A= NP_000365.3:p.Asn336=
NR_036510.1:n.1190A=
XM_005271169.1:c.791A= XP_005271226.1:p.Asn264=
XM_005271170.1:c.791A= XP_005271227.1:p.Asn264=
XM_011542080.1:c.944A= XP_011540382.1:p.Asn315=
XM_011542081.1:c.839A= XP_011540383.1:p.Asn280=
NM_000374.5:c.1007A= MANE Select NP_000365.3:p.Asn336=
NR_158184.1:n.1088A=
NR_158185.1:n.1038A=
NR_036510.2:n.1069A=