Canonical Allele Identifier: CA338748135

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404495A>T (hg19) ; chr1:g.19078001A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078001A>T , CM000663.2:g.19078001A>T	GRCh38
NC_000001.10:g.19404495A>T , CM000663.1:g.19404495A>T	GRCh37
NC_000001.9:g.19277082A>T	NCBI36
NG_027669.1:g.137252T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15299T>A MANE Select	ENSP00000364403.3:p.Val5100Asp
ENST00000375224.1:c.2420T>A	ENSP00000364372.1:p.Val807Asp
ENST00000375225.7:c.524T>A	ENSP00000364373.3:p.Val175Asp
ENST00000375254.7:c.15299T>A	ENSP00000364403.3:p.Val5100Asp
ENST00000459947.5:n.3306T>A
NM_020765.2:c.15299T>A	NP_065816.2:p.Val5100Asp
XM_011541108.1:c.15452T>A	XP_011539410.1:p.Val5151Asp
XM_011541109.1:c.15449T>A	XP_011539411.1:p.Val5150Asp
XM_011541110.1:c.15449T>A	XP_011539412.1:p.Val5150Asp
XM_011541111.1:c.15449T>A	XP_011539413.1:p.Val5150Asp
XM_011541112.1:c.15437T>A	XP_011539414.1:p.Val5146Asp
XM_011541113.1:c.15434T>A	XP_011539415.1:p.Val5145Asp
XM_011541114.1:c.15434T>A	XP_011539416.1:p.Val5145Asp
XM_011541115.1:c.15428T>A	XP_011539417.1:p.Val5143Asp
XM_011541116.1:c.15419T>A	XP_011539418.1:p.Val5140Asp
XM_011541117.1:c.15368T>A	XP_011539419.1:p.Val5123Asp
XM_011541118.1:c.15365T>A	XP_011539420.1:p.Val5122Asp
XM_011541119.1:c.15332T>A	XP_011539421.1:p.Val5111Asp
XM_011541120.1:c.15329T>A	XP_011539422.1:p.Val5110Asp
XM_011541121.1:c.15296T>A	XP_011539423.1:p.Val5099Asp
XM_011541108.3:c.15566T>A	XP_011539410.2:p.Val5189Asp
XM_011541109.3:c.15563T>A	XP_011539411.2:p.Val5188Asp
XM_011541110.3:c.15563T>A	XP_011539412.2:p.Val5188Asp
XM_011541111.3:c.15563T>A	XP_011539413.2:p.Val5188Asp
XM_011541112.3:c.15551T>A	XP_011539414.2:p.Val5184Asp
XM_011541113.3:c.15548T>A	XP_011539415.2:p.Val5183Asp
XM_011541114.3:c.15548T>A	XP_011539416.2:p.Val5183Asp
XM_011541115.3:c.15542T>A	XP_011539417.2:p.Val5181Asp
XM_011541116.3:c.15533T>A	XP_011539418.2:p.Val5178Asp
XM_011541117.3:c.15482T>A	XP_011539419.2:p.Val5161Asp
XM_011541118.3:c.15479T>A	XP_011539420.2:p.Val5160Asp
XM_011541119.3:c.15446T>A	XP_011539421.2:p.Val5149Asp
XM_011541120.3:c.15443T>A	XP_011539422.2:p.Val5148Asp
XM_011541121.3:c.15410T>A	XP_011539423.2:p.Val5137Asp
XM_017000822.2:c.15545T>A	XP_016856311.2:p.Val5182Asp
XM_017000823.2:c.15518T>A	XP_016856312.2:p.Val5173Asp
XM_017000824.2:c.15464T>A	XP_016856313.2:p.Val5155Asp
XM_017000825.2:c.15449T>A	XP_016856314.2:p.Val5150Asp
XM_017000826.2:c.15446T>A	XP_016856315.2:p.Val5149Asp
XM_017000827.2:c.15431T>A	XP_016856316.2:p.Val5144Asp
XM_017000828.2:c.15407T>A	XP_016856317.2:p.Val5136Asp
XM_017000829.2:c.15359T>A	XP_016856318.2:p.Val5120Asp
XM_017000830.2:c.15308T>A	XP_016856319.2:p.Val5103Asp
NM_020765.3:c.15299T>A MANE Select	NP_065816.2:p.Val5100Asp