Canonical Allele Identifier: CA372072226

Gene: UTP23

Linked Data

• MyVariant Identifiers: chr8:g.117783696A>T (hg19) ; chr8:g.116771457A>T (hg38)

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