Canonical Allele Identifier: CA2518506322

Gene: UTP23

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116771384_116771385insCCTCTTTA , CM000670.2:g.116771384_116771385insCCTCTTTA	GRCh38
NC_000008.10:g.117783623_117783624insCCTCTTTA , CM000670.1:g.117783623_117783624insCCTCTTTA	GRCh37
NC_000008.9:g.117852804_117852805insCCTCTTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309822.7:c.364-72_364-71insCCTCTTTA MANE Select	ENSP00000308332.2:n.364-72_364-71insCCTCTTTA
ENST00000309822.6:c.364-72_364-71insCCTCTTTA	ENSP00000308332.2:n.364-72_364-71insCCTCTTTA
ENST00000517814.1:c.363+1018_363+1019insCCTCTTTA	ENSP00000429962.1:n.363+1018_363+1019insCCTCTTTA
ENST00000517820.1:c.188+4593_188+4594insCCTCTTTA	ENSP00000427767.1:n.188+4593_188+4594insCCTCTTTA
ENST00000520733.5:c.45+1018_45+1019insCCTCTTTA	ENSP00000429384.1:n.45+1018_45+1019insCCTCTTTA
ENST00000521071.1:c.188+4593_188+4594insCCTCTTTA	ENSP00000430029.1:n.188+4593_188+4594insCCTCTTTA
ENST00000521703.5:c.188+4593_188+4594insCCTCTTTA	ENSP00000428455.1:n.188+4593_188+4594insCCTCTTTA
ENST00000521974.1:n.270-72_270-71insCCTCTTTA
ENST00000524128.1:c.45+1018_45+1019insCCTCTTTA	ENSP00000430309.1:n.45+1018_45+1019insCCTCTTTA
NM_032334.2:c.364-72_364-71insCCTCTTTA	NP_115710.2:n.364-72_364-71insCCTCTTTA
XM_005251080.2:c.363+1018_363+1019insCCTCTTTA	XP_005251137.2:n.363+1018_363+1019insCCTCTTTA
XR_928356.1:n.411+1018_411+1019insCCTCTTTA
XR_928357.1:n.411+1018_411+1019insCCTCTTTA
NM_032334.3:c.364-72_364-71insCCTCTTTA MANE Select	NP_115710.2:n.364-72_364-71insCCTCTTTA