Canonical Allele Identifier: CA2473585853
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45015394A= , CM000663.2:g.45015394A= GRCh38
NC_000001.10:g.45481066A= , CM000663.1:g.45481066A= GRCh37
NC_000001.9:g.45253653A= NCBI36
NG_007122.2:g.8237A=
NG_033058.1:g.962T=

Transcript Alleles

HGVS Amino-acid change
ENST00000246337.9:c.1000A= MANE Select ENSP00000246337.4:p.Ile334=
ENST00000491773.6:c.757A= ENSP00000498551.1:p.Ile253=
ENST00000636293.1:c.862A= ENSP00000490710.1:p.Ile288=
ENST00000636836.1:c.*36A= ENSP00000490594.1:n.*36A=
ENST00000651476.1:c.895A= ENSP00000498668.1:p.Ile299=
ENST00000652165.1:c.757A= ENSP00000498295.1:p.Ile253=
ENST00000652287.1:c.937A= ENSP00000498413.1:p.Ile313=
ENST00000652514.1:c.961A= ENSP00000498635.1:n.961A=
ENST00000246337.8:c.1000A= ENSP00000246337.4:p.Ile334=
ENST00000465678.1:n.745A=
ENST00000472254.1:n.753A=
ENST00000494399.5:n.1667A=
NM_000374.4:c.1000A= NP_000365.3:p.Ile334=
NR_036510.1:n.1183A=
XM_005271169.1:c.784A= XP_005271226.1:p.Ile262=
XM_005271170.1:c.784A= XP_005271227.1:p.Ile262=
XM_011542080.1:c.937A= XP_011540382.1:p.Ile313=
XM_011542081.1:c.832A= XP_011540383.1:p.Ile278=
NM_000374.5:c.1000A= MANE Select NP_000365.3:p.Ile334=
NR_158184.1:n.1081A=
NR_158185.1:n.1031A=
NR_036510.2:n.1062A=