Canonical Allele Identifier: CA2473585858
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45015399C= , CM000663.2:g.45015399C= GRCh38
NC_000001.10:g.45481071C= , CM000663.1:g.45481071C= GRCh37
NC_000001.9:g.45253658C= NCBI36
NG_007122.2:g.8242C=
NG_033058.1:g.957G=

Transcript Alleles

HGVS Amino-acid change
ENST00000246337.9:c.1005C= MANE Select ENSP00000246337.4:p.Ala335=
ENST00000491773.6:c.762C= ENSP00000498551.1:p.Ala254=
ENST00000636293.1:c.867C= ENSP00000490710.1:p.Ala289=
ENST00000636836.1:c.*41C= ENSP00000490594.1:n.*41C=
ENST00000651476.1:c.900C= ENSP00000498668.1:p.Ala300=
ENST00000652165.1:c.762C= ENSP00000498295.1:p.Ala254=
ENST00000652287.1:c.942C= ENSP00000498413.1:p.Ala314=
ENST00000652514.1:c.966C= ENSP00000498635.1:n.966C=
ENST00000246337.8:c.1005C= ENSP00000246337.4:p.Ala335=
ENST00000465678.1:n.750C=
ENST00000472254.1:n.758C=
ENST00000494399.5:n.1672C=
NM_000374.4:c.1005C= NP_000365.3:p.Ala335=
NR_036510.1:n.1188C=
XM_005271169.1:c.789C= XP_005271226.1:p.Ala263=
XM_005271170.1:c.789C= XP_005271227.1:p.Ala263=
XM_011542080.1:c.942C= XP_011540382.1:p.Ala314=
XM_011542081.1:c.837C= XP_011540383.1:p.Ala279=
NM_000374.5:c.1005C= MANE Select NP_000365.3:p.Ala335=
NR_158184.1:n.1086C=
NR_158185.1:n.1036C=
NR_036510.2:n.1067C=