Canonical Allele Identifier: CA378685845
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788969C>A , CM000672.2:g.125788969C>A GRCh38
NC_000010.10:g.127477538C>A , CM000672.1:g.127477538C>A GRCh37
NC_000010.9:g.127467528C>A NCBI36
NG_011557.1:g.39300G>T
NG_011557.2:g.39300G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.697G>T ENSP00000518871.1:p.Ala233Ser
ENST00000368797.10:c.697G>T MANE Select ENSP00000357787.4:p.Ala233Ser
ENST00000465577.6:c.717G>T
ENST00000648427.1:c.*695G>T ENSP00000497909.1:n.*695G>T
ENST00000649536.1:c.697G>T ENSP00000497817.1:p.Ala233Ser
ENST00000650185.1:c.847G>T
ENST00000650472.1:n.3083G>T
ENST00000650524.1:c.610G>T ENSP00000498108.1:n.610G>T
ENST00000650587.1:c.778G>T ENSP00000497366.1:p.Ala260Ser
ENST00000368786.5:c.697G>T ENSP00000357775.1:p.Ala233Ser
ENST00000368797.8:c.697G>T ENSP00000357787.4:p.Ala233Ser
ENST00000464267.1:n.794G>T
ENST00000465577.5:n.339G>T
ENST00000470483.1:n.385G>T
ENST00000484541.5:n.470G>T
ENST00000616800.4:c.161-3709G>T
ENST00000622016.4:c.241-3130G>T ENSP00000483041.1:n.241-3130G>T
NM_000375.2:c.697G>T NP_000366.1:p.Ala233Ser
XM_005270137.2:c.778G>T XP_005270194.1:p.Ala260Ser
XM_005270138.2:c.697G>T XP_005270195.1:p.Ala233Ser
XM_005270139.2:c.661-3130G>T XP_005270196.1:n.661-3130G>T
XM_006717960.2:c.778G>T XP_006718023.1:p.Ala260Ser
XM_011540127.1:c.661-3709G>T XP_011538429.1:n.661-3709G>T
XR_246103.2:n.877G>T
XR_945810.1:n.1107G>T
NM_000375.3:c.697G>T MANE Select NP_000366.1:p.Ala233Ser
NM_001324036.1:c.778G>T NP_001310965.1:p.Ala260Ser
NM_001324037.1:c.697G>T NP_001310966.1:p.Ala233Ser
NM_001324038.1:c.616G>T NP_001310967.1:p.Ala206Ser
NR_136675.1:n.782G>T
NR_136676.1:n.1209G>T
NR_136677.1:n.927-3130G>T
NR_136678.1:n.693G>T
XM_011540127.2:c.661-3709G>T XP_011538429.1:n.661-3709G>T
XM_017016611.2:c.778G>T XP_016872100.2:p.Ala260Ser
XM_017016612.2:c.661-3130G>T XP_016872101.1:n.661-3130G>T
XM_024448154.1:c.697G>T XP_024303922.1:p.Ala233Ser
XR_002957010.1:n.2036G>T
XR_246103.3:n.892G>T
XR_945810.2:n.1122G>T
NM_001324036.2:c.778G>T NP_001310965.1:p.Ala260Ser
NM_001324037.2:c.697G>T NP_001310966.1:p.Ala233Ser
NM_001324038.2:c.616G>T NP_001310967.1:p.Ala206Ser
NR_136675.2:n.772G>T
NR_136676.2:n.1199G>T
NR_136678.2:n.683G>T
NR_136677.2:n.917-3130G>T