Canonical Allele Identifier: CA340118224

Gene: UROD

Linked Data

• MyVariant Identifiers: chr1:g.45479615G>A (hg19) ; chr1:g.45013943G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45013943G>A , CM000663.2:g.45013943G>A	GRCh38
NC_000001.10:g.45479615G>A , CM000663.1:g.45479615G>A	GRCh37
NC_000001.9:g.45252202G>A	NCBI36
NG_007122.2:g.6786G>A
NG_033058.1:g.2413C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246337.9:c.509G>A MANE Select	ENSP00000246337.4:p.Gly170Asp
ENST00000434478.6:c.563G>A	ENSP00000404489.2:p.Gly188Asp
ENST00000491773.6:c.404G>A	ENSP00000498551.1:p.Gly135Asp
ENST00000636293.1:c.509G>A	ENSP00000490710.1:p.Gly170Asp
ENST00000636836.1:c.509G>A	ENSP00000490594.1:p.Gly170Asp
ENST00000651476.1:c.404G>A	ENSP00000498668.1:p.Gly135Asp
ENST00000652165.1:c.404G>A	ENSP00000498295.1:p.Gly135Asp
ENST00000652287.1:c.446G>A	ENSP00000498413.1:p.Gly149Asp
ENST00000652514.1:c.470G>A	ENSP00000498635.1:n.470G>A
ENST00000246337.8:c.509G>A	ENSP00000246337.4:p.Gly170Asp
ENST00000428106.1:c.454+152G>A
ENST00000434478.5:c.446G>A	ENSP00000404489.1:p.Gly149Asp
ENST00000460334.5:n.536G>A
ENST00000460906.5:n.643G>A
ENST00000462688.5:n.636G>A
ENST00000469548.5:n.705G>A
ENST00000473012.1:n.556G>A
ENST00000478467.5:n.512G>A
ENST00000486699.5:n.629G>A
ENST00000490385.5:n.583G>A
ENST00000491300.5:n.628G>A
ENST00000491773.5:n.663G>A
ENST00000494399.5:n.649G>A
ENST00000496439.1:n.605G>A
NM_000374.4:c.509G>A	NP_000365.3:p.Gly170Asp
NR_036510.1:n.692G>A
XM_005271169.1:c.293G>A	XP_005271226.1:p.Gly98Asp
XM_005271170.1:c.293G>A	XP_005271227.1:p.Gly98Asp
XM_011542080.1:c.446G>A	XP_011540382.1:p.Gly149Asp
XM_011542081.1:c.341G>A	XP_011540383.1:p.Gly114Asp
NM_000374.5:c.509G>A MANE Select	NP_000365.3:p.Gly170Asp
NR_158184.1:n.590G>A
NR_158185.1:n.540G>A
NR_036510.2:n.571G>A