Canonical Allele Identifier: CA417877874

Gene: UROD

Linked Data

• MyVariant Identifiers: chr1:g.45479622C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45013950C>T , CM000663.2:g.45013950C>T	GRCh38
NC_000001.10:g.45479622C>T , CM000663.1:g.45479622C>T	GRCh37
NC_000001.9:g.45252209C>T	NCBI36
NG_007122.2:g.6793C>T
NG_033058.1:g.2406G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000246337.9:c.516C>T MANE Select	ENSP00000246337.4:p.Ser172=
ENST00000434478.6:c.570C>T	ENSP00000404489.2:p.Ser190=
ENST00000491773.6:c.411C>T	ENSP00000498551.1:p.Ser137=
ENST00000636293.1:c.516C>T	ENSP00000490710.1:p.Ser172=
ENST00000636836.1:c.516C>T	ENSP00000490594.1:p.Ser172=
ENST00000651476.1:c.411C>T	ENSP00000498668.1:p.Ser137=
ENST00000652165.1:c.411C>T	ENSP00000498295.1:p.Ser137=
ENST00000652287.1:c.453C>T	ENSP00000498413.1:p.Ser151=
ENST00000652514.1:c.477C>T	ENSP00000498635.1:n.477C>T
ENST00000246337.8:c.516C>T	ENSP00000246337.4:p.Ser172=
ENST00000428106.1:c.454+159C>T
ENST00000434478.5:c.453C>T	ENSP00000404489.1:p.Ser151=
ENST00000460334.5:n.543C>T
ENST00000460906.5:n.650C>T
ENST00000462688.5:n.643C>T
ENST00000469548.5:n.712C>T
ENST00000473012.1:n.563C>T
ENST00000478467.5:n.519C>T
ENST00000486699.5:n.636C>T
ENST00000490385.5:n.590C>T
ENST00000491300.5:n.635C>T
ENST00000491773.5:n.670C>T
ENST00000494399.5:n.656C>T
ENST00000496439.1:n.612C>T
NM_000374.4:c.516C>T	NP_000365.3:p.Ser172=
NR_036510.1:n.699C>T
XM_005271169.1:c.300C>T	XP_005271226.1:p.Ser100=
XM_005271170.1:c.300C>T	XP_005271227.1:p.Ser100=
XM_011542080.1:c.453C>T	XP_011540382.1:p.Ser151=
XM_011542081.1:c.348C>T	XP_011540383.1:p.Ser116=
NM_000374.5:c.516C>T MANE Select	NP_000365.3:p.Ser172=
NR_158184.1:n.597C>T
NR_158185.1:n.547C>T
NR_036510.2:n.578C>T