Canonical Allele Identifier: CA338748344

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404553C>A (hg19) ; chr1:g.19078059C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078059C>A , CM000663.2:g.19078059C>A	GRCh38
NC_000001.10:g.19404553C>A , CM000663.1:g.19404553C>A	GRCh37
NC_000001.9:g.19277140C>A	NCBI36
NG_027669.1:g.137194G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15241G>T MANE Select	ENSP00000364403.3:p.Asp5081Tyr
ENST00000375224.1:c.2362G>T	ENSP00000364372.1:p.Asp788Tyr
ENST00000375225.7:c.466G>T	ENSP00000364373.3:p.Asp156Tyr
ENST00000375254.7:c.15241G>T	ENSP00000364403.3:p.Asp5081Tyr
ENST00000459947.5:n.3248G>T
NM_020765.2:c.15241G>T	NP_065816.2:p.Asp5081Tyr
XM_011541108.1:c.15394G>T	XP_011539410.1:p.Asp5132Tyr
XM_011541109.1:c.15391G>T	XP_011539411.1:p.Asp5131Tyr
XM_011541110.1:c.15391G>T	XP_011539412.1:p.Asp5131Tyr
XM_011541111.1:c.15391G>T	XP_011539413.1:p.Asp5131Tyr
XM_011541112.1:c.15379G>T	XP_011539414.1:p.Asp5127Tyr
XM_011541113.1:c.15376G>T	XP_011539415.1:p.Asp5126Tyr
XM_011541114.1:c.15376G>T	XP_011539416.1:p.Asp5126Tyr
XM_011541115.1:c.15370G>T	XP_011539417.1:p.Asp5124Tyr
XM_011541116.1:c.15361G>T	XP_011539418.1:p.Asp5121Tyr
XM_011541117.1:c.15310G>T	XP_011539419.1:p.Asp5104Tyr
XM_011541118.1:c.15307G>T	XP_011539420.1:p.Asp5103Tyr
XM_011541119.1:c.15274G>T	XP_011539421.1:p.Asp5092Tyr
XM_011541120.1:c.15271G>T	XP_011539422.1:p.Asp5091Tyr
XM_011541121.1:c.15238G>T	XP_011539423.1:p.Asp5080Tyr
XM_011541108.3:c.15508G>T	XP_011539410.2:p.Asp5170Tyr
XM_011541109.3:c.15505G>T	XP_011539411.2:p.Asp5169Tyr
XM_011541110.3:c.15505G>T	XP_011539412.2:p.Asp5169Tyr
XM_011541111.3:c.15505G>T	XP_011539413.2:p.Asp5169Tyr
XM_011541112.3:c.15493G>T	XP_011539414.2:p.Asp5165Tyr
XM_011541113.3:c.15490G>T	XP_011539415.2:p.Asp5164Tyr
XM_011541114.3:c.15490G>T	XP_011539416.2:p.Asp5164Tyr
XM_011541115.3:c.15484G>T	XP_011539417.2:p.Asp5162Tyr
XM_011541116.3:c.15475G>T	XP_011539418.2:p.Asp5159Tyr
XM_011541117.3:c.15424G>T	XP_011539419.2:p.Asp5142Tyr
XM_011541118.3:c.15421G>T	XP_011539420.2:p.Asp5141Tyr
XM_011541119.3:c.15388G>T	XP_011539421.2:p.Asp5130Tyr
XM_011541120.3:c.15385G>T	XP_011539422.2:p.Asp5129Tyr
XM_011541121.3:c.15352G>T	XP_011539423.2:p.Asp5118Tyr
XM_017000822.2:c.15487G>T	XP_016856311.2:p.Asp5163Tyr
XM_017000823.2:c.15460G>T	XP_016856312.2:p.Asp5154Tyr
XM_017000824.2:c.15406G>T	XP_016856313.2:p.Asp5136Tyr
XM_017000825.2:c.15391G>T	XP_016856314.2:p.Asp5131Tyr
XM_017000826.2:c.15388G>T	XP_016856315.2:p.Asp5130Tyr
XM_017000827.2:c.15373G>T	XP_016856316.2:p.Asp5125Tyr
XM_017000828.2:c.15349G>T	XP_016856317.2:p.Asp5117Tyr
XM_017000829.2:c.15301G>T	XP_016856318.2:p.Asp5101Tyr
XM_017000830.2:c.15250G>T	XP_016856319.2:p.Asp5084Tyr
NM_020765.3:c.15241G>T MANE Select	NP_065816.2:p.Asp5081Tyr