Canonical Allele Identifier: CA1943001196
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788869C= , CM000672.2:g.125788869C= GRCh38
NC_000010.10:g.127477438C= , CM000672.1:g.127477438C= GRCh37
NC_000010.9:g.127467428C= NCBI36
NG_011557.1:g.39400G=
NG_011557.2:g.39400G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.797G= ENSP00000518871.1:p.Ter266=
ENST00000368797.10:c.797G= MANE Select ENSP00000357787.4:p.Ter266=
ENST00000465577.6:c.817G=
ENST00000648427.1:c.*795G= ENSP00000497909.1:n.*795G=
ENST00000649536.1:c.797G= ENSP00000497817.1:p.Ter266=
ENST00000650472.1:n.3183G=
ENST00000650524.1:c.710G= ENSP00000498108.1:n.710G=
ENST00000650587.1:c.878G= ENSP00000497366.1:p.Ter293=
ENST00000368786.5:c.797G= ENSP00000357775.1:p.Ter266=
ENST00000368797.8:c.797G= ENSP00000357787.4:p.Ter266=
ENST00000464267.1:n.894G=
ENST00000465577.5:n.439G=
ENST00000470483.1:n.485G=
ENST00000484541.5:n.570G=
ENST00000616800.4:c.161-3609G=
ENST00000622016.4:c.241-3030G= ENSP00000483041.1:n.241-3030G=
NM_000375.2:c.797G= NP_000366.1:p.Ter266=
XM_005270137.2:c.878G= XP_005270194.1:p.Ter293=
XM_005270138.2:c.797G= XP_005270195.1:p.Ter266=
XM_005270139.2:c.661-3030G= XP_005270196.1:n.661-3030G=
XM_006717960.2:c.878G= XP_006718023.1:p.Ter293=
XM_011540127.1:c.661-3609G= XP_011538429.1:n.661-3609G=
XR_246103.2:n.977G=
XR_945810.1:n.1207G=
NM_000375.3:c.797G= MANE Select NP_000366.1:p.Ter266=
NM_001324036.1:c.878G= NP_001310965.1:p.Ter293=
NM_001324037.1:c.797G= NP_001310966.1:p.Ter266=
NM_001324038.1:c.716G= NP_001310967.1:p.Ter239=
NR_136675.1:n.882G=
NR_136676.1:n.1309G=
NR_136677.1:n.927-3030G=
NR_136678.1:n.793G=
XM_011540127.2:c.661-3609G= XP_011538429.1:n.661-3609G=
XM_017016611.2:c.878G= XP_016872100.2:p.Ter293=
XM_017016612.2:c.661-3030G= XP_016872101.1:n.661-3030G=
XM_024448154.1:c.797G= XP_024303922.1:p.Ter266=
XR_002957010.1:n.2136G=
XR_246103.3:n.992G=
XR_945810.2:n.1222G=
NM_001324036.2:c.878G= NP_001310965.1:p.Ter293=
NM_001324037.2:c.797G= NP_001310966.1:p.Ter266=
NM_001324038.2:c.716G= NP_001310967.1:p.Ter239=
NR_136675.2:n.872G=
NR_136676.2:n.1299G=
NR_136678.2:n.783G=
NR_136677.2:n.917-3030G=