Canonical Allele Identifier: CA338748184

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404514G>T (hg19) ; chr1:g.19078020G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078020G>T , CM000663.2:g.19078020G>T	GRCh38
NC_000001.10:g.19404514G>T , CM000663.1:g.19404514G>T	GRCh37
NC_000001.9:g.19277101G>T	NCBI36
NG_027669.1:g.137233C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15280C>A MANE Select	ENSP00000364403.3:p.Leu5094Ile
ENST00000375224.1:c.2401C>A	ENSP00000364372.1:p.Leu801Ile
ENST00000375225.7:c.505C>A	ENSP00000364373.3:p.Leu169Ile
ENST00000375254.7:c.15280C>A	ENSP00000364403.3:p.Leu5094Ile
ENST00000459947.5:n.3287C>A
NM_020765.2:c.15280C>A	NP_065816.2:p.Leu5094Ile
XM_011541108.1:c.15433C>A	XP_011539410.1:p.Leu5145Ile
XM_011541109.1:c.15430C>A	XP_011539411.1:p.Leu5144Ile
XM_011541110.1:c.15430C>A	XP_011539412.1:p.Leu5144Ile
XM_011541111.1:c.15430C>A	XP_011539413.1:p.Leu5144Ile
XM_011541112.1:c.15418C>A	XP_011539414.1:p.Leu5140Ile
XM_011541113.1:c.15415C>A	XP_011539415.1:p.Leu5139Ile
XM_011541114.1:c.15415C>A	XP_011539416.1:p.Leu5139Ile
XM_011541115.1:c.15409C>A	XP_011539417.1:p.Leu5137Ile
XM_011541116.1:c.15400C>A	XP_011539418.1:p.Leu5134Ile
XM_011541117.1:c.15349C>A	XP_011539419.1:p.Leu5117Ile
XM_011541118.1:c.15346C>A	XP_011539420.1:p.Leu5116Ile
XM_011541119.1:c.15313C>A	XP_011539421.1:p.Leu5105Ile
XM_011541120.1:c.15310C>A	XP_011539422.1:p.Leu5104Ile
XM_011541121.1:c.15277C>A	XP_011539423.1:p.Leu5093Ile
XM_011541108.3:c.15547C>A	XP_011539410.2:p.Leu5183Ile
XM_011541109.3:c.15544C>A	XP_011539411.2:p.Leu5182Ile
XM_011541110.3:c.15544C>A	XP_011539412.2:p.Leu5182Ile
XM_011541111.3:c.15544C>A	XP_011539413.2:p.Leu5182Ile
XM_011541112.3:c.15532C>A	XP_011539414.2:p.Leu5178Ile
XM_011541113.3:c.15529C>A	XP_011539415.2:p.Leu5177Ile
XM_011541114.3:c.15529C>A	XP_011539416.2:p.Leu5177Ile
XM_011541115.3:c.15523C>A	XP_011539417.2:p.Leu5175Ile
XM_011541116.3:c.15514C>A	XP_011539418.2:p.Leu5172Ile
XM_011541117.3:c.15463C>A	XP_011539419.2:p.Leu5155Ile
XM_011541118.3:c.15460C>A	XP_011539420.2:p.Leu5154Ile
XM_011541119.3:c.15427C>A	XP_011539421.2:p.Leu5143Ile
XM_011541120.3:c.15424C>A	XP_011539422.2:p.Leu5142Ile
XM_011541121.3:c.15391C>A	XP_011539423.2:p.Leu5131Ile
XM_017000822.2:c.15526C>A	XP_016856311.2:p.Leu5176Ile
XM_017000823.2:c.15499C>A	XP_016856312.2:p.Leu5167Ile
XM_017000824.2:c.15445C>A	XP_016856313.2:p.Leu5149Ile
XM_017000825.2:c.15430C>A	XP_016856314.2:p.Leu5144Ile
XM_017000826.2:c.15427C>A	XP_016856315.2:p.Leu5143Ile
XM_017000827.2:c.15412C>A	XP_016856316.2:p.Leu5138Ile
XM_017000828.2:c.15388C>A	XP_016856317.2:p.Leu5130Ile
XM_017000829.2:c.15340C>A	XP_016856318.2:p.Leu5114Ile
XM_017000830.2:c.15289C>A	XP_016856319.2:p.Leu5097Ile
NM_020765.3:c.15280C>A MANE Select	NP_065816.2:p.Leu5094Ile