Canonical Allele Identifier: CA1813484602

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771984_116771985delinsAC , CM000670.2:g.116771984_116771985delinsAC	GRCh38
NC_000008.10:g.117784223_117784224delinsAC , CM000670.1:g.117784223_117784224delinsAC	GRCh37
NC_000008.9:g.117853404_117853405delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.*142_*143delinsAC MANE Select	ENSP00000308332.2:n.*142_*143delinsAC
ENST00000309822.6:c.*142_*143delinsAC	ENSP00000308332.2:n.*142_*143delinsAC
ENST00000517814.1:c.363+1618_363+1619delinsAC	ENSP00000429962.1:n.363+1618_363+1619delinsAC
ENST00000517820.1:c.188+5193_188+5194delinsAC	ENSP00000427767.1:n.188+5193_188+5194delinsAC
ENST00000520733.5:c.45+1618_45+1619delinsAC	ENSP00000429384.1:n.45+1618_45+1619delinsAC
ENST00000521071.1:c.188+5193_188+5194delinsAC	ENSP00000430029.1:n.188+5193_188+5194delinsAC
ENST00000521703.5:c.188+5193_188+5194delinsAC	ENSP00000428455.1:n.188+5193_188+5194delinsAC
ENST00000524128.1:c.45+1618_45+1619delinsAC	ENSP00000430309.1:n.45+1618_45+1619delinsAC
NM_032334.2:c.*142_*143delinsAC	NP_115710.2:n.*142_*143delinsAC
XM_005251080.2:c.363+1618_363+1619delinsAC	XP_005251137.2:n.363+1618_363+1619delinsAC
XR_928356.1:n.411+1618_411+1619delinsAC
XR_928357.1:n.411+1618_411+1619delinsAC
NM_032334.3:c.*142_*143delinsAC MANE Select	NP_115710.2:n.*142_*143delinsAC