Canonical Allele Identifier: CA2507893356

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771383_116771384insTAG , CM000670.2:g.116771383_116771384insTAG	GRCh38
NC_000008.10:g.117783622_117783623insTAG , CM000670.1:g.117783622_117783623insTAG	GRCh37
NC_000008.9:g.117852803_117852804insTAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-73_364-72insTAG MANE Select	ENSP00000308332.2:n.364-73_364-72insTAG
ENST00000309822.6:c.364-73_364-72insTAG	ENSP00000308332.2:n.364-73_364-72insTAG
ENST00000517814.1:c.363+1017_363+1018insTAG	ENSP00000429962.1:n.363+1017_363+1018insTAG
ENST00000517820.1:c.188+4592_188+4593insTAG	ENSP00000427767.1:n.188+4592_188+4593insTAG
ENST00000520733.5:c.45+1017_45+1018insTAG	ENSP00000429384.1:n.45+1017_45+1018insTAG
ENST00000521071.1:c.188+4592_188+4593insTAG	ENSP00000430029.1:n.188+4592_188+4593insTAG
ENST00000521703.5:c.188+4592_188+4593insTAG	ENSP00000428455.1:n.188+4592_188+4593insTAG
ENST00000521974.1:n.270-73_270-72insTAG
ENST00000524128.1:c.45+1017_45+1018insTAG	ENSP00000430309.1:n.45+1017_45+1018insTAG
NM_032334.2:c.364-73_364-72insTAG	NP_115710.2:n.364-73_364-72insTAG
XM_005251080.2:c.363+1017_363+1018insTAG	XP_005251137.2:n.363+1017_363+1018insTAG
XR_928356.1:n.411+1017_411+1018insTAG
XR_928357.1:n.411+1017_411+1018insTAG
NM_032334.3:c.364-73_364-72insTAG MANE Select	NP_115710.2:n.364-73_364-72insTAG