Canonical Allele Identifier: CA1813483859

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771369_116771371delinsCTT , CM000670.2:g.116771369_116771371delinsCTT	GRCh38
NC_000008.10:g.117783608_117783610delinsCTT , CM000670.1:g.117783608_117783610delinsCTT	GRCh37
NC_000008.9:g.117852789_117852791delinsCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-87_364-85delinsCTT MANE Select	ENSP00000308332.2:n.364-87_364-85delinsCTT
ENST00000309822.6:c.364-87_364-85delinsCTT	ENSP00000308332.2:n.364-87_364-85delinsCTT
ENST00000517814.1:c.363+1003_363+1005delinsCTT	ENSP00000429962.1:n.363+1003_363+1005delinsCTT
ENST00000517820.1:c.188+4578_188+4580delinsCTT	ENSP00000427767.1:n.188+4578_188+4580delinsCTT
ENST00000520733.5:c.45+1003_45+1005delinsCTT	ENSP00000429384.1:n.45+1003_45+1005delinsCTT
ENST00000521071.1:c.188+4578_188+4580delinsCTT	ENSP00000430029.1:n.188+4578_188+4580delinsCTT
ENST00000521703.5:c.188+4578_188+4580delinsCTT	ENSP00000428455.1:n.188+4578_188+4580delinsCTT
ENST00000521974.1:n.270-87_270-85delinsCTT
ENST00000524128.1:c.45+1003_45+1005delinsCTT	ENSP00000430309.1:n.45+1003_45+1005delinsCTT
NM_032334.2:c.364-87_364-85delinsCTT	NP_115710.2:n.364-87_364-85delinsCTT
XM_005251080.2:c.363+1003_363+1005delinsCTT	XP_005251137.2:n.363+1003_363+1005delinsCTT
XR_928356.1:n.411+1003_411+1005delinsCTT
XR_928357.1:n.411+1003_411+1005delinsCTT
NM_032334.3:c.364-87_364-85delinsCTT MANE Select	NP_115710.2:n.364-87_364-85delinsCTT