Canonical Allele Identifier: CA338748163

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404507A>T (hg19) ; chr1:g.19078013A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078013A>T , CM000663.2:g.19078013A>T	GRCh38
NC_000001.10:g.19404507A>T , CM000663.1:g.19404507A>T	GRCh37
NC_000001.9:g.19277094A>T	NCBI36
NG_027669.1:g.137240T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15287T>A MANE Select	ENSP00000364403.3:p.Phe5096Tyr
ENST00000375224.1:c.2408T>A	ENSP00000364372.1:p.Phe803Tyr
ENST00000375225.7:c.512T>A	ENSP00000364373.3:p.Phe171Tyr
ENST00000375254.7:c.15287T>A	ENSP00000364403.3:p.Phe5096Tyr
ENST00000459947.5:n.3294T>A
NM_020765.2:c.15287T>A	NP_065816.2:p.Phe5096Tyr
XM_011541108.1:c.15440T>A	XP_011539410.1:p.Phe5147Tyr
XM_011541109.1:c.15437T>A	XP_011539411.1:p.Phe5146Tyr
XM_011541110.1:c.15437T>A	XP_011539412.1:p.Phe5146Tyr
XM_011541111.1:c.15437T>A	XP_011539413.1:p.Phe5146Tyr
XM_011541112.1:c.15425T>A	XP_011539414.1:p.Phe5142Tyr
XM_011541113.1:c.15422T>A	XP_011539415.1:p.Phe5141Tyr
XM_011541114.1:c.15422T>A	XP_011539416.1:p.Phe5141Tyr
XM_011541115.1:c.15416T>A	XP_011539417.1:p.Phe5139Tyr
XM_011541116.1:c.15407T>A	XP_011539418.1:p.Phe5136Tyr
XM_011541117.1:c.15356T>A	XP_011539419.1:p.Phe5119Tyr
XM_011541118.1:c.15353T>A	XP_011539420.1:p.Phe5118Tyr
XM_011541119.1:c.15320T>A	XP_011539421.1:p.Phe5107Tyr
XM_011541120.1:c.15317T>A	XP_011539422.1:p.Phe5106Tyr
XM_011541121.1:c.15284T>A	XP_011539423.1:p.Phe5095Tyr
XM_011541108.3:c.15554T>A	XP_011539410.2:p.Phe5185Tyr
XM_011541109.3:c.15551T>A	XP_011539411.2:p.Phe5184Tyr
XM_011541110.3:c.15551T>A	XP_011539412.2:p.Phe5184Tyr
XM_011541111.3:c.15551T>A	XP_011539413.2:p.Phe5184Tyr
XM_011541112.3:c.15539T>A	XP_011539414.2:p.Phe5180Tyr
XM_011541113.3:c.15536T>A	XP_011539415.2:p.Phe5179Tyr
XM_011541114.3:c.15536T>A	XP_011539416.2:p.Phe5179Tyr
XM_011541115.3:c.15530T>A	XP_011539417.2:p.Phe5177Tyr
XM_011541116.3:c.15521T>A	XP_011539418.2:p.Phe5174Tyr
XM_011541117.3:c.15470T>A	XP_011539419.2:p.Phe5157Tyr
XM_011541118.3:c.15467T>A	XP_011539420.2:p.Phe5156Tyr
XM_011541119.3:c.15434T>A	XP_011539421.2:p.Phe5145Tyr
XM_011541120.3:c.15431T>A	XP_011539422.2:p.Phe5144Tyr
XM_011541121.3:c.15398T>A	XP_011539423.2:p.Phe5133Tyr
XM_017000822.2:c.15533T>A	XP_016856311.2:p.Phe5178Tyr
XM_017000823.2:c.15506T>A	XP_016856312.2:p.Phe5169Tyr
XM_017000824.2:c.15452T>A	XP_016856313.2:p.Phe5151Tyr
XM_017000825.2:c.15437T>A	XP_016856314.2:p.Phe5146Tyr
XM_017000826.2:c.15434T>A	XP_016856315.2:p.Phe5145Tyr
XM_017000827.2:c.15419T>A	XP_016856316.2:p.Phe5140Tyr
XM_017000828.2:c.15395T>A	XP_016856317.2:p.Phe5132Tyr
XM_017000829.2:c.15347T>A	XP_016856318.2:p.Phe5116Tyr
XM_017000830.2:c.15296T>A	XP_016856319.2:p.Phe5099Tyr
NM_020765.3:c.15287T>A MANE Select	NP_065816.2:p.Phe5096Tyr