Canonical Allele Identifier: CA1813484125
Gene: UTP23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116771609_116771610delinsGA , CM000670.2:g.116771609_116771610delinsGA GRCh38
NC_000008.10:g.117783848_117783849delinsGA , CM000670.1:g.117783848_117783849delinsGA GRCh37
NC_000008.9:g.117853029_117853030delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309822.7:c.517_518delinsGA MANE Select ENSP00000308332.2:p.Glu173=
ENST00000309822.6:c.517_518delinsGA ENSP00000308332.2:p.Glu173=
ENST00000517814.1:c.363+1243_363+1244delinsGA ENSP00000429962.1:n.363+1243_363+1244delinsGA
ENST00000517820.1:c.188+4818_188+4819delinsGA ENSP00000427767.1:n.188+4818_188+4819delinsGA
ENST00000520733.5:c.45+1243_45+1244delinsGA ENSP00000429384.1:n.45+1243_45+1244delinsGA
ENST00000521071.1:c.188+4818_188+4819delinsGA ENSP00000430029.1:n.188+4818_188+4819delinsGA
ENST00000521703.5:c.188+4818_188+4819delinsGA ENSP00000428455.1:n.188+4818_188+4819delinsGA
ENST00000521974.1:n.423_424delinsGA
ENST00000524128.1:c.45+1243_45+1244delinsGA ENSP00000430309.1:n.45+1243_45+1244delinsGA
NM_032334.2:c.517_518delinsGA NP_115710.2:p.Glu173=
XM_005251080.2:c.363+1243_363+1244delinsGA XP_005251137.2:n.363+1243_363+1244delinsGA
XR_928356.1:n.411+1243_411+1244delinsGA
XR_928357.1:n.411+1243_411+1244delinsGA
NM_032334.3:c.517_518delinsGA MANE Select NP_115710.2:p.Glu173=