Canonical Allele Identifier: CA338748177

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404513A>C (hg19) ; chr1:g.19078019A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078019A>C , CM000663.2:g.19078019A>C	GRCh38
NC_000001.10:g.19404513A>C , CM000663.1:g.19404513A>C	GRCh37
NC_000001.9:g.19277100A>C	NCBI36
NG_027669.1:g.137234T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15281T>G MANE Select	ENSP00000364403.3:p.Leu5094Arg
ENST00000375224.1:c.2402T>G	ENSP00000364372.1:p.Leu801Arg
ENST00000375225.7:c.506T>G	ENSP00000364373.3:p.Leu169Arg
ENST00000375254.7:c.15281T>G	ENSP00000364403.3:p.Leu5094Arg
ENST00000459947.5:n.3288T>G
NM_020765.2:c.15281T>G	NP_065816.2:p.Leu5094Arg
XM_011541108.1:c.15434T>G	XP_011539410.1:p.Leu5145Arg
XM_011541109.1:c.15431T>G	XP_011539411.1:p.Leu5144Arg
XM_011541110.1:c.15431T>G	XP_011539412.1:p.Leu5144Arg
XM_011541111.1:c.15431T>G	XP_011539413.1:p.Leu5144Arg
XM_011541112.1:c.15419T>G	XP_011539414.1:p.Leu5140Arg
XM_011541113.1:c.15416T>G	XP_011539415.1:p.Leu5139Arg
XM_011541114.1:c.15416T>G	XP_011539416.1:p.Leu5139Arg
XM_011541115.1:c.15410T>G	XP_011539417.1:p.Leu5137Arg
XM_011541116.1:c.15401T>G	XP_011539418.1:p.Leu5134Arg
XM_011541117.1:c.15350T>G	XP_011539419.1:p.Leu5117Arg
XM_011541118.1:c.15347T>G	XP_011539420.1:p.Leu5116Arg
XM_011541119.1:c.15314T>G	XP_011539421.1:p.Leu5105Arg
XM_011541120.1:c.15311T>G	XP_011539422.1:p.Leu5104Arg
XM_011541121.1:c.15278T>G	XP_011539423.1:p.Leu5093Arg
XM_011541108.3:c.15548T>G	XP_011539410.2:p.Leu5183Arg
XM_011541109.3:c.15545T>G	XP_011539411.2:p.Leu5182Arg
XM_011541110.3:c.15545T>G	XP_011539412.2:p.Leu5182Arg
XM_011541111.3:c.15545T>G	XP_011539413.2:p.Leu5182Arg
XM_011541112.3:c.15533T>G	XP_011539414.2:p.Leu5178Arg
XM_011541113.3:c.15530T>G	XP_011539415.2:p.Leu5177Arg
XM_011541114.3:c.15530T>G	XP_011539416.2:p.Leu5177Arg
XM_011541115.3:c.15524T>G	XP_011539417.2:p.Leu5175Arg
XM_011541116.3:c.15515T>G	XP_011539418.2:p.Leu5172Arg
XM_011541117.3:c.15464T>G	XP_011539419.2:p.Leu5155Arg
XM_011541118.3:c.15461T>G	XP_011539420.2:p.Leu5154Arg
XM_011541119.3:c.15428T>G	XP_011539421.2:p.Leu5143Arg
XM_011541120.3:c.15425T>G	XP_011539422.2:p.Leu5142Arg
XM_011541121.3:c.15392T>G	XP_011539423.2:p.Leu5131Arg
XM_017000822.2:c.15527T>G	XP_016856311.2:p.Leu5176Arg
XM_017000823.2:c.15500T>G	XP_016856312.2:p.Leu5167Arg
XM_017000824.2:c.15446T>G	XP_016856313.2:p.Leu5149Arg
XM_017000825.2:c.15431T>G	XP_016856314.2:p.Leu5144Arg
XM_017000826.2:c.15428T>G	XP_016856315.2:p.Leu5143Arg
XM_017000827.2:c.15413T>G	XP_016856316.2:p.Leu5138Arg
XM_017000828.2:c.15389T>G	XP_016856317.2:p.Leu5130Arg
XM_017000829.2:c.15341T>G	XP_016856318.2:p.Leu5114Arg
XM_017000830.2:c.15290T>G	XP_016856319.2:p.Leu5097Arg
NM_020765.3:c.15281T>G MANE Select	NP_065816.2:p.Leu5094Arg