Canonical Allele Identifier: CA378685890
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788989G>C , CM000672.2:g.125788989G>C GRCh38
NC_000010.10:g.127477558G>C , CM000672.1:g.127477558G>C GRCh37
NC_000010.9:g.127467548G>C NCBI36
NG_011557.1:g.39280C>G
NG_011557.2:g.39280C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.677C>G ENSP00000518871.1:p.Pro226Arg
ENST00000368797.10:c.677C>G MANE Select ENSP00000357787.4:p.Pro226Arg
ENST00000465577.6:c.697C>G
ENST00000648427.1:c.*675C>G ENSP00000497909.1:n.*675C>G
ENST00000649536.1:c.677C>G ENSP00000497817.1:p.Pro226Arg
ENST00000650185.1:c.827C>G
ENST00000650472.1:n.3063C>G
ENST00000650524.1:c.590C>G ENSP00000498108.1:n.590C>G
ENST00000650587.1:c.758C>G ENSP00000497366.1:p.Pro253Arg
ENST00000368786.5:c.677C>G ENSP00000357775.1:p.Pro226Arg
ENST00000368797.8:c.677C>G ENSP00000357787.4:p.Pro226Arg
ENST00000464267.1:n.774C>G
ENST00000465577.5:n.319C>G
ENST00000470483.1:n.365C>G
ENST00000484541.5:n.450C>G
ENST00000616800.4:c.161-3729C>G
ENST00000622016.4:c.241-3150C>G ENSP00000483041.1:n.241-3150C>G
NM_000375.2:c.677C>G NP_000366.1:p.Pro226Arg
XM_005270137.2:c.758C>G XP_005270194.1:p.Pro253Arg
XM_005270138.2:c.677C>G XP_005270195.1:p.Pro226Arg
XM_005270139.2:c.661-3150C>G XP_005270196.1:n.661-3150C>G
XM_006717960.2:c.758C>G XP_006718023.1:p.Pro253Arg
XM_011540127.1:c.661-3729C>G XP_011538429.1:n.661-3729C>G
XR_246103.2:n.857C>G
XR_945810.1:n.1087C>G
NM_000375.3:c.677C>G MANE Select NP_000366.1:p.Pro226Arg
NM_001324036.1:c.758C>G NP_001310965.1:p.Pro253Arg
NM_001324037.1:c.677C>G NP_001310966.1:p.Pro226Arg
NM_001324038.1:c.596C>G NP_001310967.1:p.Pro199Arg
NR_136675.1:n.762C>G
NR_136676.1:n.1189C>G
NR_136677.1:n.927-3150C>G
NR_136678.1:n.673C>G
XM_011540127.2:c.661-3729C>G XP_011538429.1:n.661-3729C>G
XM_017016611.2:c.758C>G XP_016872100.2:p.Pro253Arg
XM_017016612.2:c.661-3150C>G XP_016872101.1:n.661-3150C>G
XM_024448154.1:c.677C>G XP_024303922.1:p.Pro226Arg
XR_002957010.1:n.2016C>G
XR_246103.3:n.872C>G
XR_945810.2:n.1102C>G
NM_001324036.2:c.758C>G NP_001310965.1:p.Pro253Arg
NM_001324037.2:c.677C>G NP_001310966.1:p.Pro226Arg
NM_001324038.2:c.596C>G NP_001310967.1:p.Pro199Arg
NR_136675.2:n.752C>G
NR_136676.2:n.1179C>G
NR_136678.2:n.663C>G
NR_136677.2:n.917-3150C>G