Canonical Allele Identifier: CA1943013956
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823119_125823140delinsGAGCAATGACAACAGGGGCGGA , CM000672.2:g.125823119_125823140delinsGAGCAATGACAACAGGGGCGGA GRCh38
NC_000010.10:g.127511688_127511709delinsGAGCAATGACAACAGGGGCGGA , CM000672.1:g.127511688_127511709delinsGAGCAATGACAACAGGGGCGGA GRCh37
NC_000010.9:g.127501678_127501699delinsGAGCAATGACAACAGGGGCGGA NCBI36
NG_011557.1:g.5129_5150delinsTCCGCCCCTGTTGTCATTGCTC
NG_029095.1:g.4585_4606delinsGAGCAATGACAACAGGGGCGGA
NG_011557.2:g.5129_5150delinsTCCGCCCCTGTTGTCATTGCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000518871.1:n.-138_-117delinsTCCGCC...
ENST00000368797.10:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC MANE Select ENSP00000357787.4:n.-138_-117delinsTCCGCC...
ENST00000648119.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000497494.1:n.-138_-117delinsTCCGCC...
ENST00000648427.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000497909.1:n.-138_-117delinsTCCGCC...
ENST00000649536.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000497817.1:n.-138_-117delinsTCCGCC...
ENST00000368778.7:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000357767.3:n.-138_-117delinsTCCGCC...
ENST00000368797.8:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000357787.4:n.-138_-117delinsTCCGCC...
ENST00000420761.5:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC ENSP00000414833.1:n.-138_-117delinsTCCGCC...
NM_000375.2:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_000366.1:n.-138_-117delinsTCCGCCCCTGTT...
XM_006717960.2:c.-27+67_-27+88delinsTCCGCCCCTGTTGTCATTGCTC XP_006718023.1:n.-27+67_-27+88delinsTCCGC...
NM_000375.3:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC MANE Select NP_000366.1:n.-138_-117delinsTCCGCCCCTGTT...
NM_001324036.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310965.1:n.-138_-117delinsTCCGCCCCT...
NM_001324037.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310966.1:n.-138_-117delinsTCCGCCCCT...
NM_001324038.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310967.1:n.-138_-117delinsTCCGCCCCT...
NM_001324039.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310968.1:n.-138_-117delinsTCCGCCCCT...
NR_136675.1:n.129_150delinsTCCGCCCCTGTTGTCATTGCTC
NR_136676.1:n.129_150delinsTCCGCCCCTGTTGTCATTGCTC
NR_136677.1:n.129_150delinsTCCGCCCCTGTTGTCATTGCTC
NR_136678.1:n.129_150delinsTCCGCCCCTGTTGTCATTGCTC
XM_017016611.2:c.-27+67_-27+88delinsTCCGCCCCTGTTGTCATTGCTC XP_016872100.2:n.-27+67_-27+88delinsTCCGC...
XM_024448154.1:c.-27+67_-27+88delinsTCCGCCCCTGTTGTCATTGCTC XP_024303922.1:n.-27+67_-27+88delinsTCCGC...
XM_024448155.1:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC XP_024303923.1:n.-138_-117delinsTCCGCCCCT...
XR_002957010.1:n.38+67_38+88delinsTCCGCCCCTGTTGTCATTGCTC
NM_001324036.2:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310965.1:n.-138_-117delinsTCCGCCCCT...
NM_001324037.2:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310966.1:n.-138_-117delinsTCCGCCCCT...
NM_001324038.2:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310967.1:n.-138_-117delinsTCCGCCCCT...
NR_136675.2:n.119_140delinsTCCGCCCCTGTTGTCATTGCTC
NR_136676.2:n.119_140delinsTCCGCCCCTGTTGTCATTGCTC
NR_136678.2:n.119_140delinsTCCGCCCCTGTTGTCATTGCTC
NM_001324039.2:c.-138_-117delinsTCCGCCCCTGTTGTCATTGCTC NP_001310968.1:n.-138_-117delinsTCCGCCCCT...
NR_136677.2:n.119_140delinsTCCGCCCCTGTTGTCATTGCTC