Canonical Allele Identifier: CA1813484076
Gene: UTP23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116771586A= , CM000670.2:g.116771586A= GRCh38
NC_000008.10:g.117783825A= , CM000670.1:g.117783825A= GRCh37
NC_000008.9:g.117853006A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000309822.7:c.494A= MANE Select ENSP00000308332.2:p.Gln165=
ENST00000309822.6:c.494A= ENSP00000308332.2:p.Gln165=
ENST00000517814.1:c.363+1220A= ENSP00000429962.1:n.363+1220A=
ENST00000517820.1:c.188+4795A= ENSP00000427767.1:n.188+4795A=
ENST00000520733.5:c.45+1220A= ENSP00000429384.1:n.45+1220A=
ENST00000521071.1:c.188+4795A= ENSP00000430029.1:n.188+4795A=
ENST00000521703.5:c.188+4795A= ENSP00000428455.1:n.188+4795A=
ENST00000521974.1:n.400A=
ENST00000524128.1:c.45+1220A= ENSP00000430309.1:n.45+1220A=
NM_032334.2:c.494A= NP_115710.2:p.Gln165=
XM_005251080.2:c.363+1220A= XP_005251137.2:n.363+1220A=
XR_928356.1:n.411+1220A=
XR_928357.1:n.411+1220A=
NM_032334.3:c.494A= MANE Select NP_115710.2:p.Gln165=