Canonical Allele Identifier: CA1630848527

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125823221G= , CM000672.2:g.125823221G=	GRCh38
NC_000010.10:g.127511790G= , CM000672.1:g.127511790G=	GRCh37
NC_000010.9:g.127501780G=	NCBI36
NG_011557.1:g.5048C=
NG_029095.1:g.4687G=
NG_011557.2:g.5048C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000375.3:c.-219C= MANE Select	NP_000366.1:n.-219C=
ENST00000368797.10:c.-219C= MANE Select	ENSP00000357787.4:n.-219C=
NM_000375.2:c.-219C=	NP_000366.1:n.-219C=
NM_001324036.1:c.-219C=	NP_001310965.1:n.-219C=
NM_001324036.2:c.-219C=	NP_001310965.1:n.-219C=
NM_001324037.1:c.-219C=	NP_001310966.1:n.-219C=
NM_001324037.2:c.-219C=	NP_001310966.1:n.-219C=
NM_001324038.1:c.-219C=	NP_001310967.1:n.-219C=
NM_001324038.2:c.-219C=	NP_001310967.1:n.-219C=
NM_001324039.1:c.-219C=	NP_001310968.1:n.-219C=
NM_001324039.2:c.-219C=	NP_001310968.1:n.-219C=
NR_136675.1:n.48C=
NR_136675.2:n.38C=
NR_136676.1:n.48C=
NR_136676.2:n.38C=
NR_136677.1:n.48C=
NR_136677.2:n.38C=
NR_136678.1:n.48C=
NR_136678.2:n.38C=
ENST00000368797.8:c.-219C=	ENSP00000357787.4:n.-219C=
ENST00000420761.5:c.-219C=	ENSP00000414833.1:n.-219C=
ENST00000713579.1:c.-219C=	ENSP00000518871.1:n.-219C=
XM_006717960.2:c.-41C=	XP_006718023.1:n.-41C=
XM_017016611.2:c.-41C=	XP_016872100.2:n.-41C=
XM_024448154.1:c.-41C=	XP_024303922.1:n.-41C=
XM_024448155.1:c.-219C=	XP_024303923.1:n.-219C=
XR_002957010.1:n.24C=