Canonical Allele Identifier: CA338748188

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404516G>T (hg19) ; chr1:g.19078022G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078022G>T , CM000663.2:g.19078022G>T	GRCh38
NC_000001.10:g.19404516G>T , CM000663.1:g.19404516G>T	GRCh37
NC_000001.9:g.19277103G>T	NCBI36
NG_027669.1:g.137231C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15278C>A MANE Select	ENSP00000364403.3:p.Ser5093Tyr
ENST00000375224.1:c.2399C>A	ENSP00000364372.1:p.Ser800Tyr
ENST00000375225.7:c.503C>A	ENSP00000364373.3:p.Ser168Tyr
ENST00000375254.7:c.15278C>A	ENSP00000364403.3:p.Ser5093Tyr
ENST00000459947.5:n.3285C>A
NM_020765.2:c.15278C>A	NP_065816.2:p.Ser5093Tyr
XM_011541108.1:c.15431C>A	XP_011539410.1:p.Ser5144Tyr
XM_011541109.1:c.15428C>A	XP_011539411.1:p.Ser5143Tyr
XM_011541110.1:c.15428C>A	XP_011539412.1:p.Ser5143Tyr
XM_011541111.1:c.15428C>A	XP_011539413.1:p.Ser5143Tyr
XM_011541112.1:c.15416C>A	XP_011539414.1:p.Ser5139Tyr
XM_011541113.1:c.15413C>A	XP_011539415.1:p.Ser5138Tyr
XM_011541114.1:c.15413C>A	XP_011539416.1:p.Ser5138Tyr
XM_011541115.1:c.15407C>A	XP_011539417.1:p.Ser5136Tyr
XM_011541116.1:c.15398C>A	XP_011539418.1:p.Ser5133Tyr
XM_011541117.1:c.15347C>A	XP_011539419.1:p.Ser5116Tyr
XM_011541118.1:c.15344C>A	XP_011539420.1:p.Ser5115Tyr
XM_011541119.1:c.15311C>A	XP_011539421.1:p.Ser5104Tyr
XM_011541120.1:c.15308C>A	XP_011539422.1:p.Ser5103Tyr
XM_011541121.1:c.15275C>A	XP_011539423.1:p.Ser5092Tyr
XM_011541108.3:c.15545C>A	XP_011539410.2:p.Ser5182Tyr
XM_011541109.3:c.15542C>A	XP_011539411.2:p.Ser5181Tyr
XM_011541110.3:c.15542C>A	XP_011539412.2:p.Ser5181Tyr
XM_011541111.3:c.15542C>A	XP_011539413.2:p.Ser5181Tyr
XM_011541112.3:c.15530C>A	XP_011539414.2:p.Ser5177Tyr
XM_011541113.3:c.15527C>A	XP_011539415.2:p.Ser5176Tyr
XM_011541114.3:c.15527C>A	XP_011539416.2:p.Ser5176Tyr
XM_011541115.3:c.15521C>A	XP_011539417.2:p.Ser5174Tyr
XM_011541116.3:c.15512C>A	XP_011539418.2:p.Ser5171Tyr
XM_011541117.3:c.15461C>A	XP_011539419.2:p.Ser5154Tyr
XM_011541118.3:c.15458C>A	XP_011539420.2:p.Ser5153Tyr
XM_011541119.3:c.15425C>A	XP_011539421.2:p.Ser5142Tyr
XM_011541120.3:c.15422C>A	XP_011539422.2:p.Ser5141Tyr
XM_011541121.3:c.15389C>A	XP_011539423.2:p.Ser5130Tyr
XM_017000822.2:c.15524C>A	XP_016856311.2:p.Ser5175Tyr
XM_017000823.2:c.15497C>A	XP_016856312.2:p.Ser5166Tyr
XM_017000824.2:c.15443C>A	XP_016856313.2:p.Ser5148Tyr
XM_017000825.2:c.15428C>A	XP_016856314.2:p.Ser5143Tyr
XM_017000826.2:c.15425C>A	XP_016856315.2:p.Ser5142Tyr
XM_017000827.2:c.15410C>A	XP_016856316.2:p.Ser5137Tyr
XM_017000828.2:c.15386C>A	XP_016856317.2:p.Ser5129Tyr
XM_017000829.2:c.15338C>A	XP_016856318.2:p.Ser5113Tyr
XM_017000830.2:c.15287C>A	XP_016856319.2:p.Ser5096Tyr
NM_020765.3:c.15278C>A MANE Select	NP_065816.2:p.Ser5093Tyr