Canonical Allele Identifier: CA2781877062

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771928_116771929insAG , CM000670.2:g.116771928_116771929insAG	GRCh38
NC_000008.10:g.117784167_117784168insAG , CM000670.1:g.117784167_117784168insAG	GRCh37
NC_000008.9:g.117853348_117853349insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.*86_*87insAG MANE Select	ENSP00000308332.2:n.*86_*87insAG
ENST00000309822.6:c.*86_*87insAG	ENSP00000308332.2:n.*86_*87insAG
ENST00000517814.1:c.363+1562_363+1563insAG	ENSP00000429962.1:n.363+1562_363+1563insAG
ENST00000517820.1:c.188+5137_188+5138insAG	ENSP00000427767.1:n.188+5137_188+5138insAG
ENST00000520733.5:c.45+1562_45+1563insAG	ENSP00000429384.1:n.45+1562_45+1563insAG
ENST00000521071.1:c.188+5137_188+5138insAG	ENSP00000430029.1:n.188+5137_188+5138insAG
ENST00000521703.5:c.188+5137_188+5138insAG	ENSP00000428455.1:n.188+5137_188+5138insAG
ENST00000524128.1:c.45+1562_45+1563insAG	ENSP00000430309.1:n.45+1562_45+1563insAG
NM_032334.2:c.*86_*87insAG	NP_115710.2:n.*86_*87insAG
XM_005251080.2:c.363+1562_363+1563insAG	XP_005251137.2:n.363+1562_363+1563insAG
XR_928356.1:n.411+1562_411+1563insAG
XR_928357.1:n.411+1562_411+1563insAG
NM_032334.3:c.*86_*87insAG MANE Select	NP_115710.2:n.*86_*87insAG