Canonical Allele Identifier: CA338748333

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404551A>T (hg19) ; chr1:g.19078057A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078057A>T , CM000663.2:g.19078057A>T	GRCh38
NC_000001.10:g.19404551A>T , CM000663.1:g.19404551A>T	GRCh37
NC_000001.9:g.19277138A>T	NCBI36
NG_027669.1:g.137196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15243T>A MANE Select	ENSP00000364403.3:p.Asp5081Glu
ENST00000375224.1:c.2364T>A	ENSP00000364372.1:p.Asp788Glu
ENST00000375225.7:c.468T>A	ENSP00000364373.3:p.Asp156Glu
ENST00000375254.7:c.15243T>A	ENSP00000364403.3:p.Asp5081Glu
ENST00000459947.5:n.3250T>A
NM_020765.2:c.15243T>A	NP_065816.2:p.Asp5081Glu
XM_011541108.1:c.15396T>A	XP_011539410.1:p.Asp5132Glu
XM_011541109.1:c.15393T>A	XP_011539411.1:p.Asp5131Glu
XM_011541110.1:c.15393T>A	XP_011539412.1:p.Asp5131Glu
XM_011541111.1:c.15393T>A	XP_011539413.1:p.Asp5131Glu
XM_011541112.1:c.15381T>A	XP_011539414.1:p.Asp5127Glu
XM_011541113.1:c.15378T>A	XP_011539415.1:p.Asp5126Glu
XM_011541114.1:c.15378T>A	XP_011539416.1:p.Asp5126Glu
XM_011541115.1:c.15372T>A	XP_011539417.1:p.Asp5124Glu
XM_011541116.1:c.15363T>A	XP_011539418.1:p.Asp5121Glu
XM_011541117.1:c.15312T>A	XP_011539419.1:p.Asp5104Glu
XM_011541118.1:c.15309T>A	XP_011539420.1:p.Asp5103Glu
XM_011541119.1:c.15276T>A	XP_011539421.1:p.Asp5092Glu
XM_011541120.1:c.15273T>A	XP_011539422.1:p.Asp5091Glu
XM_011541121.1:c.15240T>A	XP_011539423.1:p.Asp5080Glu
XM_011541108.3:c.15510T>A	XP_011539410.2:p.Asp5170Glu
XM_011541109.3:c.15507T>A	XP_011539411.2:p.Asp5169Glu
XM_011541110.3:c.15507T>A	XP_011539412.2:p.Asp5169Glu
XM_011541111.3:c.15507T>A	XP_011539413.2:p.Asp5169Glu
XM_011541112.3:c.15495T>A	XP_011539414.2:p.Asp5165Glu
XM_011541113.3:c.15492T>A	XP_011539415.2:p.Asp5164Glu
XM_011541114.3:c.15492T>A	XP_011539416.2:p.Asp5164Glu
XM_011541115.3:c.15486T>A	XP_011539417.2:p.Asp5162Glu
XM_011541116.3:c.15477T>A	XP_011539418.2:p.Asp5159Glu
XM_011541117.3:c.15426T>A	XP_011539419.2:p.Asp5142Glu
XM_011541118.3:c.15423T>A	XP_011539420.2:p.Asp5141Glu
XM_011541119.3:c.15390T>A	XP_011539421.2:p.Asp5130Glu
XM_011541120.3:c.15387T>A	XP_011539422.2:p.Asp5129Glu
XM_011541121.3:c.15354T>A	XP_011539423.2:p.Asp5118Glu
XM_017000822.2:c.15489T>A	XP_016856311.2:p.Asp5163Glu
XM_017000823.2:c.15462T>A	XP_016856312.2:p.Asp5154Glu
XM_017000824.2:c.15408T>A	XP_016856313.2:p.Asp5136Glu
XM_017000825.2:c.15393T>A	XP_016856314.2:p.Asp5131Glu
XM_017000826.2:c.15390T>A	XP_016856315.2:p.Asp5130Glu
XM_017000827.2:c.15375T>A	XP_016856316.2:p.Asp5125Glu
XM_017000828.2:c.15351T>A	XP_016856317.2:p.Asp5117Glu
XM_017000829.2:c.15303T>A	XP_016856318.2:p.Asp5101Glu
XM_017000830.2:c.15252T>A	XP_016856319.2:p.Asp5084Glu
NM_020765.3:c.15243T>A MANE Select	NP_065816.2:p.Asp5081Glu