Canonical Allele Identifier: CA2688329612

Gene: UTP23

Linked Data

• gnomAD v4: 8-116771349-A-AAAAAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771355_116771359dup , CM000670.2:g.116771355_116771359dup	GRCh38
NC_000008.10:g.117783594_117783598dup , CM000670.1:g.117783594_117783598dup	GRCh37
NC_000008.9:g.117852775_117852779dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-101_364-97dup MANE Select	ENSP00000308332.2:n.364-101_364-97dup
ENST00000309822.6:c.364-101_364-97dup	ENSP00000308332.2:n.364-101_364-97dup
ENST00000517814.1:c.363+989_363+993dup	ENSP00000429962.1:n.363+989_363+993dup
ENST00000517820.1:c.188+4564_188+4568dup	ENSP00000427767.1:n.188+4564_188+4568dup
ENST00000520733.5:c.45+989_45+993dup	ENSP00000429384.1:n.45+989_45+993dup
ENST00000521071.1:c.188+4564_188+4568dup	ENSP00000430029.1:n.188+4564_188+4568dup
ENST00000521703.5:c.188+4564_188+4568dup	ENSP00000428455.1:n.188+4564_188+4568dup
ENST00000521974.1:n.270-101_270-97dup
ENST00000524128.1:c.45+989_45+993dup	ENSP00000430309.1:n.45+989_45+993dup
NM_032334.2:c.364-101_364-97dup	NP_115710.2:n.364-101_364-97dup
XM_005251080.2:c.363+989_363+993dup	XP_005251137.2:n.363+989_363+993dup
XR_928356.1:n.411+989_411+993dup
XR_928357.1:n.411+989_411+993dup
NM_032334.3:c.364-101_364-97dup MANE Select	NP_115710.2:n.364-101_364-97dup