Canonical Allele Identifier: CA1813483784

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771265_116771267delinsCTG , CM000670.2:g.116771265_116771267delinsCTG	GRCh38
NC_000008.10:g.117783504_117783506delinsCTG , CM000670.1:g.117783504_117783506delinsCTG	GRCh37
NC_000008.9:g.117852685_117852687delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-191_364-189delinsCTG MANE Select	ENSP00000308332.2:n.364-191_364-189delinsCTG
ENST00000309822.6:c.364-191_364-189delinsCTG	ENSP00000308332.2:n.364-191_364-189delinsCTG
ENST00000517814.1:c.363+899_363+901delinsCTG	ENSP00000429962.1:n.363+899_363+901delinsCTG
ENST00000517820.1:c.188+4474_188+4476delinsCTG	ENSP00000427767.1:n.188+4474_188+4476delinsCTG
ENST00000520733.5:c.45+899_45+901delinsCTG	ENSP00000429384.1:n.45+899_45+901delinsCTG
ENST00000521071.1:c.188+4474_188+4476delinsCTG	ENSP00000430029.1:n.188+4474_188+4476delinsCTG
ENST00000521703.5:c.188+4474_188+4476delinsCTG	ENSP00000428455.1:n.188+4474_188+4476delinsCTG
ENST00000521974.1:n.270-191_270-189delinsCTG
ENST00000524128.1:c.45+899_45+901delinsCTG	ENSP00000430309.1:n.45+899_45+901delinsCTG
NM_032334.2:c.364-191_364-189delinsCTG	NP_115710.2:n.364-191_364-189delinsCTG
XM_005251080.2:c.363+899_363+901delinsCTG	XP_005251137.2:n.363+899_363+901delinsCTG
XR_928356.1:n.411+899_411+901delinsCTG
XR_928357.1:n.411+899_411+901delinsCTG
NM_032334.3:c.364-191_364-189delinsCTG MANE Select	NP_115710.2:n.364-191_364-189delinsCTG