Canonical Allele Identifier: CA372072226
Gene: UTP23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.116771457A>T , CM000670.2:g.116771457A>T GRCh38
NC_000008.10:g.117783696A>T , CM000670.1:g.117783696A>T GRCh37
NC_000008.9:g.117852877A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000309822.7:c.365A>T MANE Select ENSP00000308332.2:p.Asp122Val
ENST00000309822.6:c.365A>T ENSP00000308332.2:p.Asp122Val
ENST00000517814.1:c.363+1091A>T ENSP00000429962.1:n.363+1091A>T
ENST00000517820.1:c.188+4666A>T ENSP00000427767.1:n.188+4666A>T
ENST00000520733.5:c.45+1091A>T ENSP00000429384.1:n.45+1091A>T
ENST00000521071.1:c.188+4666A>T ENSP00000430029.1:n.188+4666A>T
ENST00000521703.5:c.188+4666A>T ENSP00000428455.1:n.188+4666A>T
ENST00000521974.1:n.271A>T
ENST00000524128.1:c.45+1091A>T ENSP00000430309.1:n.45+1091A>T
NM_032334.2:c.365A>T NP_115710.2:p.Asp122Val
XM_005251080.2:c.363+1091A>T XP_005251137.2:n.363+1091A>T
XR_928356.1:n.411+1091A>T
XR_928357.1:n.411+1091A>T
NM_032334.3:c.365A>T MANE Select NP_115710.2:p.Asp122Val