Canonical Allele Identifier: CA661187014
Gene: UROS HGNC NCBI

Linked Data

dbSNP Id: rs1473426394

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823166_125823173del , CM000672.2:g.125823166_125823173del GRCh38
NC_000010.10:g.127511735_127511742del , CM000672.1:g.127511735_127511742del GRCh37
NC_000010.9:g.127501725_127501732del NCBI36
NG_011557.1:g.5098_5105del
NG_029095.1:g.4632_4639del
NG_011557.2:g.5098_5105del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.-169_-162del ENSP00000518871.1:n.-169_-162del
ENST00000368797.10:c.-169_-162del MANE Select ENSP00000357787.4:n.-169_-162del
ENST00000648119.1:c.-169_-162del ENSP00000497494.1:n.-169_-162del
ENST00000648427.1:c.-169_-162del ENSP00000497909.1:n.-169_-162del
ENST00000649536.1:c.-169_-162del ENSP00000497817.1:n.-169_-162del
ENST00000368778.7:c.-169_-162del ENSP00000357767.3:n.-169_-162del
ENST00000368797.8:c.-169_-162del ENSP00000357787.4:n.-169_-162del
ENST00000420761.5:c.-169_-162del ENSP00000414833.1:n.-169_-162del
NM_000375.2:c.-169_-162del NP_000366.1:n.-169_-162del
XM_006717960.2:c.-27+36_-27+43del XP_006718023.1:n.-27+36_-27+43del
NM_000375.3:c.-169_-162del MANE Select NP_000366.1:n.-169_-162del
NM_001324036.1:c.-169_-162del NP_001310965.1:n.-169_-162del
NM_001324037.1:c.-169_-162del NP_001310966.1:n.-169_-162del
NM_001324038.1:c.-169_-162del NP_001310967.1:n.-169_-162del
NM_001324039.1:c.-169_-162del NP_001310968.1:n.-169_-162del
NR_136675.1:n.98_105del
NR_136676.1:n.98_105del
NR_136677.1:n.98_105del
NR_136678.1:n.98_105del
XM_017016611.2:c.-27+36_-27+43del XP_016872100.2:n.-27+36_-27+43del
XM_024448154.1:c.-27+36_-27+43del XP_024303922.1:n.-27+36_-27+43del
XM_024448155.1:c.-169_-162del XP_024303923.1:n.-169_-162del
XR_002957010.1:n.38+36_38+43del
NM_001324036.2:c.-169_-162del NP_001310965.1:n.-169_-162del
NM_001324037.2:c.-169_-162del NP_001310966.1:n.-169_-162del
NM_001324038.2:c.-169_-162del NP_001310967.1:n.-169_-162del
NR_136675.2:n.88_95del
NR_136676.2:n.88_95del
NR_136678.2:n.88_95del
NM_001324039.2:c.-169_-162del NP_001310968.1:n.-169_-162del
NR_136677.2:n.88_95del