Canonical Allele Identifier: CA1943001165
Gene: UROS HGNC NCBI

Linked Data

dbSNP Id: rs1850714712

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788815C>G , CM000672.2:g.125788815C>G GRCh38
NC_000010.10:g.127477384C>G , CM000672.1:g.127477384C>G GRCh37
NC_000010.9:g.127467374C>G NCBI36
NG_011557.1:g.39454G>C
NG_011557.2:g.39454G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.*53G>C ENSP00000518871.1:n.*53G>C
ENST00000368797.10:c.*53G>C MANE Select ENSP00000357787.4:n.*53G>C
ENST00000465577.6:c.871G>C
ENST00000648427.1:c.*849G>C ENSP00000497909.1:n.*849G>C
ENST00000649536.1:c.*53G>C ENSP00000497817.1:n.*53G>C
ENST00000650472.1:n.3237G>C
ENST00000650524.1:c.764G>C ENSP00000498108.1:n.764G>C
ENST00000650587.1:c.*53G>C ENSP00000497366.1:n.*53G>C
ENST00000368786.5:c.*53G>C ENSP00000357775.1:n.*53G>C
ENST00000368797.8:c.*53G>C ENSP00000357787.4:n.*53G>C
ENST00000464267.1:n.948G>C
ENST00000465577.5:n.493G>C
ENST00000470483.1:n.539G>C
ENST00000484541.5:n.624G>C
ENST00000616800.4:c.161-3555G>C
ENST00000622016.4:c.241-2976G>C ENSP00000483041.1:n.241-2976G>C
NM_000375.2:c.*53G>C NP_000366.1:n.*53G>C
XM_005270137.2:c.*53G>C XP_005270194.1:n.*53G>C
XM_005270138.2:c.*53G>C XP_005270195.1:n.*53G>C
XM_005270139.2:c.661-2976G>C XP_005270196.1:n.661-2976G>C
XM_006717960.2:c.*53G>C XP_006718023.1:n.*53G>C
XM_011540127.1:c.661-3555G>C XP_011538429.1:n.661-3555G>C
XR_246103.2:n.1031G>C
XR_945810.1:n.1261G>C
NM_000375.3:c.*53G>C MANE Select NP_000366.1:n.*53G>C
NM_001324036.1:c.*53G>C NP_001310965.1:n.*53G>C
NM_001324037.1:c.*53G>C NP_001310966.1:n.*53G>C
NM_001324038.1:c.*53G>C NP_001310967.1:n.*53G>C
NR_136675.1:n.936G>C
NR_136676.1:n.1363G>C
NR_136677.1:n.927-2976G>C
NR_136678.1:n.847G>C
XM_011540127.2:c.661-3555G>C XP_011538429.1:n.661-3555G>C
XM_017016611.2:c.*53G>C XP_016872100.2:n.*53G>C
XM_017016612.2:c.661-2976G>C XP_016872101.1:n.661-2976G>C
XM_024448154.1:c.*53G>C XP_024303922.1:n.*53G>C
XR_002957010.1:n.2190G>C
XR_246103.3:n.1046G>C
XR_945810.2:n.1276G>C
NM_001324036.2:c.*53G>C NP_001310965.1:n.*53G>C
NM_001324037.2:c.*53G>C NP_001310966.1:n.*53G>C
NM_001324038.2:c.*53G>C NP_001310967.1:n.*53G>C
NR_136675.2:n.926G>C
NR_136676.2:n.1353G>C
NR_136678.2:n.837G>C
NR_136677.2:n.917-2976G>C