Canonical Allele Identifier: CA1943001130
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788752G= , CM000672.2:g.125788752G= GRCh38
NC_000010.10:g.127477321G= , CM000672.1:g.127477321G= GRCh37
NC_000010.9:g.127467311G= NCBI36
NG_011557.1:g.39517C=
NG_011557.2:g.39517C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.*116C= ENSP00000518871.1:n.*116C=
ENST00000368797.10:c.*116C= MANE Select ENSP00000357787.4:n.*116C=
ENST00000465577.6:c.934C=
ENST00000648427.1:c.*912C= ENSP00000497909.1:n.*912C=
ENST00000649536.1:c.*116C= ENSP00000497817.1:n.*116C=
ENST00000650472.1:n.3300C=
ENST00000650524.1:c.827C= ENSP00000498108.1:n.827C=
ENST00000650587.1:c.*116C= ENSP00000497366.1:n.*116C=
ENST00000368786.5:c.*116C= ENSP00000357775.1:n.*116C=
ENST00000368797.8:c.*116C= ENSP00000357787.4:n.*116C=
ENST00000464267.1:n.1011C=
ENST00000465577.5:n.556C=
ENST00000470483.1:n.602C=
ENST00000484541.5:n.687C=
ENST00000616800.4:c.161-3492C=
ENST00000622016.4:c.241-2913C= ENSP00000483041.1:n.241-2913C=
NM_000375.2:c.*116C= NP_000366.1:n.*116C=
XM_005270137.2:c.*116C= XP_005270194.1:n.*116C=
XM_005270138.2:c.*116C= XP_005270195.1:n.*116C=
XM_005270139.2:c.661-2913C= XP_005270196.1:n.661-2913C=
XM_006717960.2:c.*116C= XP_006718023.1:n.*116C=
XM_011540127.1:c.661-3492C= XP_011538429.1:n.661-3492C=
XR_246103.2:n.1094C=
XR_945810.1:n.1324C=
NM_000375.3:c.*116C= MANE Select NP_000366.1:n.*116C=
NM_001324036.1:c.*116C= NP_001310965.1:n.*116C=
NM_001324037.1:c.*116C= NP_001310966.1:n.*116C=
NM_001324038.1:c.*116C= NP_001310967.1:n.*116C=
NR_136675.1:n.999C=
NR_136676.1:n.1426C=
NR_136677.1:n.927-2913C=
NR_136678.1:n.910C=
XM_011540127.2:c.661-3492C= XP_011538429.1:n.661-3492C=
XM_017016611.2:c.*116C= XP_016872100.2:n.*116C=
XM_017016612.2:c.661-2913C= XP_016872101.1:n.661-2913C=
XM_024448154.1:c.*116C= XP_024303922.1:n.*116C=
XR_002957010.1:n.2253C=
XR_246103.3:n.1109C=
XR_945810.2:n.1339C=
NM_001324036.2:c.*116C= NP_001310965.1:n.*116C=
NM_001324037.2:c.*116C= NP_001310966.1:n.*116C=
NM_001324038.2:c.*116C= NP_001310967.1:n.*116C=
NR_136675.2:n.989C=
NR_136676.2:n.1416C=
NR_136678.2:n.900C=
NR_136677.2:n.917-2913C=