Canonical Allele Identifier: CA378685878
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788983G>C , CM000672.2:g.125788983G>C GRCh38
NC_000010.10:g.127477552G>C , CM000672.1:g.127477552G>C GRCh37
NC_000010.9:g.127467542G>C NCBI36
NG_011557.1:g.39286C>G
NG_011557.2:g.39286C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.683C>G ENSP00000518871.1:p.Thr228Arg
ENST00000368797.10:c.683C>G MANE Select ENSP00000357787.4:p.Thr228Arg
ENST00000465577.6:c.703C>G
ENST00000648427.1:c.*681C>G ENSP00000497909.1:n.*681C>G
ENST00000649536.1:c.683C>G ENSP00000497817.1:p.Thr228Arg
ENST00000650185.1:c.833C>G
ENST00000650472.1:n.3069C>G
ENST00000650524.1:c.596C>G ENSP00000498108.1:n.596C>G
ENST00000650587.1:c.764C>G ENSP00000497366.1:p.Thr255Arg
ENST00000368786.5:c.683C>G ENSP00000357775.1:p.Thr228Arg
ENST00000368797.8:c.683C>G ENSP00000357787.4:p.Thr228Arg
ENST00000464267.1:n.780C>G
ENST00000465577.5:n.325C>G
ENST00000470483.1:n.371C>G
ENST00000484541.5:n.456C>G
ENST00000616800.4:c.161-3723C>G
ENST00000622016.4:c.241-3144C>G ENSP00000483041.1:n.241-3144C>G
NM_000375.2:c.683C>G NP_000366.1:p.Thr228Arg
XM_005270137.2:c.764C>G XP_005270194.1:p.Thr255Arg
XM_005270138.2:c.683C>G XP_005270195.1:p.Thr228Arg
XM_005270139.2:c.661-3144C>G XP_005270196.1:n.661-3144C>G
XM_006717960.2:c.764C>G XP_006718023.1:p.Thr255Arg
XM_011540127.1:c.661-3723C>G XP_011538429.1:n.661-3723C>G
XR_246103.2:n.863C>G
XR_945810.1:n.1093C>G
NM_000375.3:c.683C>G MANE Select NP_000366.1:p.Thr228Arg
NM_001324036.1:c.764C>G NP_001310965.1:p.Thr255Arg
NM_001324037.1:c.683C>G NP_001310966.1:p.Thr228Arg
NM_001324038.1:c.602C>G NP_001310967.1:p.Thr201Arg
NR_136675.1:n.768C>G
NR_136676.1:n.1195C>G
NR_136677.1:n.927-3144C>G
NR_136678.1:n.679C>G
XM_011540127.2:c.661-3723C>G XP_011538429.1:n.661-3723C>G
XM_017016611.2:c.764C>G XP_016872100.2:p.Thr255Arg
XM_017016612.2:c.661-3144C>G XP_016872101.1:n.661-3144C>G
XM_024448154.1:c.683C>G XP_024303922.1:p.Thr228Arg
XR_002957010.1:n.2022C>G
XR_246103.3:n.878C>G
XR_945810.2:n.1108C>G
NM_001324036.2:c.764C>G NP_001310965.1:p.Thr255Arg
NM_001324037.2:c.683C>G NP_001310966.1:p.Thr228Arg
NM_001324038.2:c.602C>G NP_001310967.1:p.Thr201Arg
NR_136675.2:n.758C>G
NR_136676.2:n.1185C>G
NR_136678.2:n.669C>G
NR_136677.2:n.917-3144C>G