Canonical Allele Identifier: CA1943013986
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823163_125823167delinsAGGGG , CM000672.2:g.125823163_125823167delinsAGGGG GRCh38
NC_000010.10:g.127511732_127511736delinsAGGGG , CM000672.1:g.127511732_127511736delinsAGGGG GRCh37
NC_000010.9:g.127501722_127501726delinsAGGGG NCBI36
NG_011557.1:g.5102_5106delinsCCCCT
NG_029095.1:g.4629_4633delinsAGGGG
NG_011557.2:g.5102_5106delinsCCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.-165_-161delinsCCCCT ENSP00000518871.1:n.-165_-161delinsCCCCT
ENST00000368797.10:c.-165_-161delinsCCCCT MANE Select ENSP00000357787.4:n.-165_-161delinsCCCCT
ENST00000648119.1:c.-165_-161delinsCCCCT ENSP00000497494.1:n.-165_-161delinsCCCCT
ENST00000648427.1:c.-165_-161delinsCCCCT ENSP00000497909.1:n.-165_-161delinsCCCCT
ENST00000649536.1:c.-165_-161delinsCCCCT ENSP00000497817.1:n.-165_-161delinsCCCCT
ENST00000368778.7:c.-165_-161delinsCCCCT ENSP00000357767.3:n.-165_-161delinsCCCCT
ENST00000368797.8:c.-165_-161delinsCCCCT ENSP00000357787.4:n.-165_-161delinsCCCCT
ENST00000420761.5:c.-165_-161delinsCCCCT ENSP00000414833.1:n.-165_-161delinsCCCCT
NM_000375.2:c.-165_-161delinsCCCCT NP_000366.1:n.-165_-161delinsCCCCT
XM_006717960.2:c.-27+40_-27+44delinsCCCCT XP_006718023.1:n.-27+40_-27+44delinsCCCCT
NM_000375.3:c.-165_-161delinsCCCCT MANE Select NP_000366.1:n.-165_-161delinsCCCCT
NM_001324036.1:c.-165_-161delinsCCCCT NP_001310965.1:n.-165_-161delinsCCCCT
NM_001324037.1:c.-165_-161delinsCCCCT NP_001310966.1:n.-165_-161delinsCCCCT
NM_001324038.1:c.-165_-161delinsCCCCT NP_001310967.1:n.-165_-161delinsCCCCT
NM_001324039.1:c.-165_-161delinsCCCCT NP_001310968.1:n.-165_-161delinsCCCCT
NR_136675.1:n.102_106delinsCCCCT
NR_136676.1:n.102_106delinsCCCCT
NR_136677.1:n.102_106delinsCCCCT
NR_136678.1:n.102_106delinsCCCCT
XM_017016611.2:c.-27+40_-27+44delinsCCCCT XP_016872100.2:n.-27+40_-27+44delinsCCCCT
XM_024448154.1:c.-27+40_-27+44delinsCCCCT XP_024303922.1:n.-27+40_-27+44delinsCCCCT
XM_024448155.1:c.-165_-161delinsCCCCT XP_024303923.1:n.-165_-161delinsCCCCT
XR_002957010.1:n.38+40_38+44delinsCCCCT
NM_001324036.2:c.-165_-161delinsCCCCT NP_001310965.1:n.-165_-161delinsCCCCT
NM_001324037.2:c.-165_-161delinsCCCCT NP_001310966.1:n.-165_-161delinsCCCCT
NM_001324038.2:c.-165_-161delinsCCCCT NP_001310967.1:n.-165_-161delinsCCCCT
NR_136675.2:n.92_96delinsCCCCT
NR_136676.2:n.92_96delinsCCCCT
NR_136678.2:n.92_96delinsCCCCT
NM_001324039.2:c.-165_-161delinsCCCCT NP_001310968.1:n.-165_-161delinsCCCCT
NR_136677.2:n.92_96delinsCCCCT