Canonical Allele Identifier: CA1140888466

Gene: UROD

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45015501G= , CM000663.2:g.45015501G=	GRCh38
NC_000001.10:g.45481173G= , CM000663.1:g.45481173G=	GRCh37
NC_000001.9:g.45253760G=	NCBI36
NG_007122.2:g.8344G=
NG_033058.1:g.855C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246337.9:c.*3G= MANE Select	ENSP00000246337.4:n.*3G=
ENST00000491773.6:c.*3G=	ENSP00000498551.1:n.*3G=
ENST00000636293.1:c.*3G=	ENSP00000490710.1:n.*3G=
ENST00000636836.1:c.*143G=	ENSP00000490594.1:n.*143G=
ENST00000651476.1:c.*3G=	ENSP00000498668.1:n.*3G=
ENST00000652165.1:c.*3G=	ENSP00000498295.1:n.*3G=
ENST00000652287.1:c.*3G=	ENSP00000498413.1:n.*3G=
ENST00000652514.1:c.1068G=	ENSP00000498635.1:n.1068G=
ENST00000246337.8:c.*3G=	ENSP00000246337.4:n.*3G=
ENST00000472254.1:n.860G=
ENST00000494399.5:n.1774G=
NM_000374.4:c.*3G=	NP_000365.3:n.*3G=
NR_036510.1:n.1290G=
XM_005271169.1:c.*3G=	XP_005271226.1:n.*3G=
XM_005271170.1:c.*3G=	XP_005271227.1:n.*3G=
XM_011542080.1:c.*3G=	XP_011540382.1:n.*3G=
XM_011542081.1:c.*3G=	XP_011540383.1:n.*3G=
NM_000374.5:c.*3G= MANE Select	NP_000365.3:n.*3G=
NR_158184.1:n.1188G=
NR_158185.1:n.1138G=
NR_036510.2:n.1169G=