Canonical Allele Identifier: CA2562485113

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771392_116771397del , CM000670.2:g.116771392_116771397del	GRCh38
NC_000008.10:g.117783631_117783636del , CM000670.1:g.117783631_117783636del	GRCh37
NC_000008.9:g.117852812_117852817del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-64_364-59del MANE Select	ENSP00000308332.2:n.364-64_364-59del
ENST00000309822.6:c.364-64_364-59del	ENSP00000308332.2:n.364-64_364-59del
ENST00000517814.1:c.363+1026_363+1031del	ENSP00000429962.1:n.363+1026_363+1031del
ENST00000517820.1:c.188+4601_188+4606del	ENSP00000427767.1:n.188+4601_188+4606del
ENST00000520733.5:c.45+1026_45+1031del	ENSP00000429384.1:n.45+1026_45+1031del
ENST00000521071.1:c.188+4601_188+4606del	ENSP00000430029.1:n.188+4601_188+4606del
ENST00000521703.5:c.188+4601_188+4606del	ENSP00000428455.1:n.188+4601_188+4606del
ENST00000521974.1:n.270-64_270-59del
ENST00000524128.1:c.45+1026_45+1031del	ENSP00000430309.1:n.45+1026_45+1031del
NM_032334.2:c.364-64_364-59del	NP_115710.2:n.364-64_364-59del
XM_005251080.2:c.363+1026_363+1031del	XP_005251137.2:n.363+1026_363+1031del
XR_928356.1:n.411+1026_411+1031del
XR_928357.1:n.411+1026_411+1031del
NM_032334.3:c.364-64_364-59del MANE Select	NP_115710.2:n.364-64_364-59del