Canonical Allele Identifier: CA2645372099

Gene: UROD

Linked Data

• gnomAD v4: 1-45013818-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45013818G>A , CM000663.2:g.45013818G>A	GRCh38
NC_000001.10:g.45479490G>A , CM000663.1:g.45479490G>A	GRCh37
NC_000001.9:g.45252077G>A	NCBI36
NG_007122.2:g.6661G>A
NG_033058.1:g.2538C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246337.9:c.474+27G>A MANE Select	ENSP00000246337.4:n.474+27G>A
ENST00000434478.6:c.528+27G>A	ENSP00000404489.2:n.528+27G>A
ENST00000491773.6:c.369+27G>A	ENSP00000498551.1:n.369+27G>A
ENST00000636293.1:c.474+27G>A	ENSP00000490710.1:n.474+27G>A
ENST00000636836.1:c.474+27G>A	ENSP00000490594.1:n.474+27G>A
ENST00000651476.1:c.369+27G>A	ENSP00000498668.1:n.369+27G>A
ENST00000652165.1:c.369+27G>A	ENSP00000498295.1:n.369+27G>A
ENST00000652287.1:c.411+27G>A	ENSP00000498413.1:n.411+27G>A
ENST00000652514.1:c.435+27G>A	ENSP00000498635.1:n.435+27G>A
ENST00000246337.8:c.474+27G>A	ENSP00000246337.4:n.474+27G>A
ENST00000428106.1:c.454+27G>A
ENST00000434478.5:c.411+27G>A	ENSP00000404489.1:n.411+27G>A
ENST00000460334.5:n.501+27G>A
ENST00000460906.5:n.518G>A
ENST00000462688.5:n.601+27G>A
ENST00000463092.5:n.897G>A
ENST00000469548.5:n.670+27G>A
ENST00000473012.1:n.521+27G>A
ENST00000478467.5:n.477+27G>A
ENST00000486699.5:n.594+27G>A
ENST00000490385.5:n.548+27G>A
ENST00000491300.5:n.593+27G>A
ENST00000491773.5:n.628+27G>A
ENST00000494399.5:n.614+27G>A
ENST00000496439.1:n.480G>A
NM_000374.4:c.474+27G>A	NP_000365.3:n.474+27G>A
NR_036510.1:n.657+27G>A
XM_005271169.1:c.258+27G>A	XP_005271226.1:n.258+27G>A
XM_005271170.1:c.258+27G>A	XP_005271227.1:n.258+27G>A
XM_011542080.1:c.411+27G>A	XP_011540382.1:n.411+27G>A
XM_011542081.1:c.306+27G>A	XP_011540383.1:n.306+27G>A
NM_000374.5:c.474+27G>A MANE Select	NP_000365.3:n.474+27G>A
NR_158184.1:n.555+27G>A
NR_158185.1:n.505+27G>A
NR_036510.2:n.536+27G>A