Canonical Allele Identifier: CA2473585696
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45015007G= , CM000663.2:g.45015007G= GRCh38
NC_000001.10:g.45480679G= , CM000663.1:g.45480679G= GRCh37
NC_000001.9:g.45253266G= NCBI36
NG_007122.2:g.7850G=
NG_033058.1:g.1349C=

Transcript Alleles

HGVS Amino-acid change
ENST00000246337.9:c.942+1G= MANE Select ENSP00000246337.4:n.942+1G=
ENST00000491773.6:c.699+1G= ENSP00000498551.1:n.699+1G=
ENST00000636293.1:c.804+1G= ENSP00000490710.1:n.804+1G=
ENST00000636836.1:c.875+171G= ENSP00000490594.1:n.875+171G=
ENST00000651476.1:c.837+1G= ENSP00000498668.1:n.837+1G=
ENST00000652165.1:c.699+1G= ENSP00000498295.1:n.699+1G=
ENST00000652287.1:c.879+1G= ENSP00000498413.1:n.879+1G=
ENST00000652514.1:c.903+1G= ENSP00000498635.1:n.903+1G=
ENST00000246337.8:c.942+1G= ENSP00000246337.4:n.942+1G=
ENST00000465678.1:n.358G=
ENST00000466193.1:n.468+1G=
ENST00000472254.1:n.695+1G=
ENST00000494399.5:n.1609+1G=
NM_000374.4:c.942+1G= NP_000365.3:n.942+1G=
NR_036510.1:n.1125+1G=
XM_005271169.1:c.726+1G= XP_005271226.1:n.726+1G=
XM_005271170.1:c.726+1G= XP_005271227.1:n.726+1G=
XM_011542080.1:c.879+1G= XP_011540382.1:n.879+1G=
XM_011542081.1:c.774+1G= XP_011540383.1:n.774+1G=
NM_000374.5:c.942+1G= MANE Select NP_000365.3:n.942+1G=
NR_158184.1:n.1023+1G=
NR_158185.1:n.973+1G=
NR_036510.2:n.1004+1G=