Canonical Allele Identifier: CA1943001228
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788923G= , CM000672.2:g.125788923G= GRCh38
NC_000010.10:g.127477492G= , CM000672.1:g.127477492G= GRCh37
NC_000010.9:g.127467482G= NCBI36
NG_011557.1:g.39346C=
NG_011557.2:g.39346C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.743C= ENSP00000518871.1:p.Pro248=
ENST00000368797.10:c.743C= MANE Select ENSP00000357787.4:p.Pro248=
ENST00000465577.6:c.763C=
ENST00000648427.1:c.*741C= ENSP00000497909.1:n.*741C=
ENST00000649536.1:c.743C= ENSP00000497817.1:p.Pro248=
ENST00000650185.1:c.893C=
ENST00000650472.1:n.3129C=
ENST00000650524.1:c.656C= ENSP00000498108.1:n.656C=
ENST00000650587.1:c.824C= ENSP00000497366.1:p.Pro275=
ENST00000368786.5:c.743C= ENSP00000357775.1:p.Pro248=
ENST00000368797.8:c.743C= ENSP00000357787.4:p.Pro248=
ENST00000464267.1:n.840C=
ENST00000465577.5:n.385C=
ENST00000470483.1:n.431C=
ENST00000484541.5:n.516C=
ENST00000616800.4:c.161-3663C=
ENST00000622016.4:c.241-3084C= ENSP00000483041.1:n.241-3084C=
NM_000375.2:c.743C= NP_000366.1:p.Pro248=
XM_005270137.2:c.824C= XP_005270194.1:p.Pro275=
XM_005270138.2:c.743C= XP_005270195.1:p.Pro248=
XM_005270139.2:c.661-3084C= XP_005270196.1:n.661-3084C=
XM_006717960.2:c.824C= XP_006718023.1:p.Pro275=
XM_011540127.1:c.661-3663C= XP_011538429.1:n.661-3663C=
XR_246103.2:n.923C=
XR_945810.1:n.1153C=
NM_000375.3:c.743C= MANE Select NP_000366.1:p.Pro248=
NM_001324036.1:c.824C= NP_001310965.1:p.Pro275=
NM_001324037.1:c.743C= NP_001310966.1:p.Pro248=
NM_001324038.1:c.662C= NP_001310967.1:p.Pro221=
NR_136675.1:n.828C=
NR_136676.1:n.1255C=
NR_136677.1:n.927-3084C=
NR_136678.1:n.739C=
XM_011540127.2:c.661-3663C= XP_011538429.1:n.661-3663C=
XM_017016611.2:c.824C= XP_016872100.2:p.Pro275=
XM_017016612.2:c.661-3084C= XP_016872101.1:n.661-3084C=
XM_024448154.1:c.743C= XP_024303922.1:p.Pro248=
XR_002957010.1:n.2082C=
XR_246103.3:n.938C=
XR_945810.2:n.1168C=
NM_001324036.2:c.824C= NP_001310965.1:p.Pro275=
NM_001324037.2:c.743C= NP_001310966.1:p.Pro248=
NM_001324038.2:c.662C= NP_001310967.1:p.Pro221=
NR_136675.2:n.818C=
NR_136676.2:n.1245C=
NR_136678.2:n.729C=
NR_136677.2:n.917-3084C=