Canonical Allele Identifier: CA1943001163

Gene: UROS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.125788812A= , CM000672.2:g.125788812A=	GRCh38
NC_000010.10:g.127477381A= , CM000672.1:g.127477381A=	GRCh37
NC_000010.9:g.127467371A=	NCBI36
NG_011557.1:g.39457T=
NG_011557.2:g.39457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000713579.1:c.*56T=	ENSP00000518871.1:n.*56T=
ENST00000368797.10:c.*56T= MANE Select	ENSP00000357787.4:n.*56T=
ENST00000465577.6:c.874T=
ENST00000648427.1:c.*852T=	ENSP00000497909.1:n.*852T=
ENST00000649536.1:c.*56T=	ENSP00000497817.1:n.*56T=
ENST00000650472.1:n.3240T=
ENST00000650524.1:c.767T=	ENSP00000498108.1:n.767T=
ENST00000650587.1:c.*56T=	ENSP00000497366.1:n.*56T=
ENST00000368786.5:c.*56T=	ENSP00000357775.1:n.*56T=
ENST00000368797.8:c.*56T=	ENSP00000357787.4:n.*56T=
ENST00000464267.1:n.951T=
ENST00000465577.5:n.496T=
ENST00000470483.1:n.542T=
ENST00000484541.5:n.627T=
ENST00000616800.4:c.161-3552T=
ENST00000622016.4:c.241-2973T=	ENSP00000483041.1:n.241-2973T=
NM_000375.2:c.*56T=	NP_000366.1:n.*56T=
XM_005270137.2:c.*56T=	XP_005270194.1:n.*56T=
XM_005270138.2:c.*56T=	XP_005270195.1:n.*56T=
XM_005270139.2:c.661-2973T=	XP_005270196.1:n.661-2973T=
XM_006717960.2:c.*56T=	XP_006718023.1:n.*56T=
XM_011540127.1:c.661-3552T=	XP_011538429.1:n.661-3552T=
XR_246103.2:n.1034T=
XR_945810.1:n.1264T=
NM_000375.3:c.*56T= MANE Select	NP_000366.1:n.*56T=
NM_001324036.1:c.*56T=	NP_001310965.1:n.*56T=
NM_001324037.1:c.*56T=	NP_001310966.1:n.*56T=
NM_001324038.1:c.*56T=	NP_001310967.1:n.*56T=
NR_136675.1:n.939T=
NR_136676.1:n.1366T=
NR_136677.1:n.927-2973T=
NR_136678.1:n.850T=
XM_011540127.2:c.661-3552T=	XP_011538429.1:n.661-3552T=
XM_017016611.2:c.*56T=	XP_016872100.2:n.*56T=
XM_017016612.2:c.661-2973T=	XP_016872101.1:n.661-2973T=
XM_024448154.1:c.*56T=	XP_024303922.1:n.*56T=
XR_002957010.1:n.2193T=
XR_246103.3:n.1049T=
XR_945810.2:n.1279T=
NM_001324036.2:c.*56T=	NP_001310965.1:n.*56T=
NM_001324037.2:c.*56T=	NP_001310966.1:n.*56T=
NM_001324038.2:c.*56T=	NP_001310967.1:n.*56T=
NR_136675.2:n.929T=
NR_136676.2:n.1356T=
NR_136678.2:n.840T=
NR_136677.2:n.917-2973T=