Canonical Allele Identifier: CA1943013959

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125823121G= , CM000672.2:g.125823121G=	GRCh38
NC_000010.10:g.127511690G= , CM000672.1:g.127511690G=	GRCh37
NC_000010.9:g.127501680G=	NCBI36
NG_011557.1:g.5148C=
NG_029095.1:g.4587G=
NG_011557.2:g.5148C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000713579.1:c.-119C=	ENSP00000518871.1:n.-119C=
ENST00000368797.10:c.-119C= MANE Select	ENSP00000357787.4:n.-119C=
ENST00000648119.1:c.-119C=	ENSP00000497494.1:n.-119C=
ENST00000648427.1:c.-119C=	ENSP00000497909.1:n.-119C=
ENST00000649536.1:c.-119C=	ENSP00000497817.1:n.-119C=
ENST00000368778.7:c.-119C=	ENSP00000357767.3:n.-119C=
ENST00000368797.8:c.-119C=	ENSP00000357787.4:n.-119C=
ENST00000420761.5:c.-119C=	ENSP00000414833.1:n.-119C=
NM_000375.2:c.-119C=	NP_000366.1:n.-119C=
XM_006717960.2:c.-27+86C=	XP_006718023.1:n.-27+86C=
NM_000375.3:c.-119C= MANE Select	NP_000366.1:n.-119C=
NM_001324036.1:c.-119C=	NP_001310965.1:n.-119C=
NM_001324037.1:c.-119C=	NP_001310966.1:n.-119C=
NM_001324038.1:c.-119C=	NP_001310967.1:n.-119C=
NM_001324039.1:c.-119C=	NP_001310968.1:n.-119C=
NR_136675.1:n.148C=
NR_136676.1:n.148C=
NR_136677.1:n.148C=
NR_136678.1:n.148C=
XM_005270140.5:c.-119C=	XP_005270197.1:n.-119C=
XM_011540127.2:c.-119C=	XP_011538429.1:n.-119C=
XM_017016611.2:c.-27+86C=	XP_016872100.2:n.-27+86C=
XM_017016612.2:c.-119C=	XP_016872101.1:n.-119C=
XM_024448154.1:c.-27+86C=	XP_024303922.1:n.-27+86C=
XM_024448155.1:c.-119C=	XP_024303923.1:n.-119C=
XR_001747196.2:n.5C=
XR_001747197.2:n.5C=
XR_002957009.1:n.5C=
XR_002957010.1:n.38+86C=
XR_246103.3:n.5C=
XR_945810.2:n.5C=
NM_001324036.2:c.-119C=	NP_001310965.1:n.-119C=
NM_001324037.2:c.-119C=	NP_001310966.1:n.-119C=
NM_001324038.2:c.-119C=	NP_001310967.1:n.-119C=
NR_136675.2:n.138C=
NR_136676.2:n.138C=
NR_136678.2:n.138C=
NM_001324039.2:c.-119C=	NP_001310968.1:n.-119C=
NR_136677.2:n.138C=