Canonical Allele Identifier: CA378685895
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788992C>A , CM000672.2:g.125788992C>A GRCh38
NC_000010.10:g.127477561C>A , CM000672.1:g.127477561C>A GRCh37
NC_000010.9:g.127467551C>A NCBI36
NG_011557.1:g.39277G>T
NG_011557.2:g.39277G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.674G>T ENSP00000518871.1:p.Gly225Val
ENST00000368797.10:c.674G>T MANE Select ENSP00000357787.4:p.Gly225Val
ENST00000465577.6:c.694G>T
ENST00000648427.1:c.*672G>T ENSP00000497909.1:n.*672G>T
ENST00000649536.1:c.674G>T ENSP00000497817.1:p.Gly225Val
ENST00000650185.1:c.824G>T
ENST00000650472.1:n.3060G>T
ENST00000650524.1:c.587G>T ENSP00000498108.1:n.587G>T
ENST00000650587.1:c.755G>T ENSP00000497366.1:p.Gly252Val
ENST00000368786.5:c.674G>T ENSP00000357775.1:p.Gly225Val
ENST00000368797.8:c.674G>T ENSP00000357787.4:p.Gly225Val
ENST00000464267.1:n.771G>T
ENST00000465577.5:n.316G>T
ENST00000470483.1:n.362G>T
ENST00000484541.5:n.447G>T
ENST00000616800.4:c.161-3732G>T
ENST00000622016.4:c.241-3153G>T ENSP00000483041.1:n.241-3153G>T
NM_000375.2:c.674G>T NP_000366.1:p.Gly225Val
XM_005270137.2:c.755G>T XP_005270194.1:p.Gly252Val
XM_005270138.2:c.674G>T XP_005270195.1:p.Gly225Val
XM_005270139.2:c.661-3153G>T XP_005270196.1:n.661-3153G>T
XM_006717960.2:c.755G>T XP_006718023.1:p.Gly252Val
XM_011540127.1:c.661-3732G>T XP_011538429.1:n.661-3732G>T
XR_246103.2:n.854G>T
XR_945810.1:n.1084G>T
NM_000375.3:c.674G>T MANE Select NP_000366.1:p.Gly225Val
NM_001324036.1:c.755G>T NP_001310965.1:p.Gly252Val
NM_001324037.1:c.674G>T NP_001310966.1:p.Gly225Val
NM_001324038.1:c.593G>T NP_001310967.1:p.Gly198Val
NR_136675.1:n.759G>T
NR_136676.1:n.1186G>T
NR_136677.1:n.927-3153G>T
NR_136678.1:n.670G>T
XM_011540127.2:c.661-3732G>T XP_011538429.1:n.661-3732G>T
XM_017016611.2:c.755G>T XP_016872100.2:p.Gly252Val
XM_017016612.2:c.661-3153G>T XP_016872101.1:n.661-3153G>T
XM_024448154.1:c.674G>T XP_024303922.1:p.Gly225Val
XR_002957010.1:n.2013G>T
XR_246103.3:n.869G>T
XR_945810.2:n.1099G>T
NM_001324036.2:c.755G>T NP_001310965.1:p.Gly252Val
NM_001324037.2:c.674G>T NP_001310966.1:p.Gly225Val
NM_001324038.2:c.593G>T NP_001310967.1:p.Gly198Val
NR_136675.2:n.749G>T
NR_136676.2:n.1176G>T
NR_136678.2:n.660G>T
NR_136677.2:n.917-3153G>T