Canonical Allele Identifier: CA338748302

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404543A>G (hg19) ; chr1:g.19078049A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078049A>G , CM000663.2:g.19078049A>G	GRCh38
NC_000001.10:g.19404543A>G , CM000663.1:g.19404543A>G	GRCh37
NC_000001.9:g.19277130A>G	NCBI36
NG_027669.1:g.137204T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15251T>C MANE Select	ENSP00000364403.3:p.Val5084Ala
ENST00000375224.1:c.2372T>C	ENSP00000364372.1:p.Val791Ala
ENST00000375225.7:c.476T>C	ENSP00000364373.3:p.Val159Ala
ENST00000375254.7:c.15251T>C	ENSP00000364403.3:p.Val5084Ala
ENST00000459947.5:n.3258T>C
NM_020765.2:c.15251T>C	NP_065816.2:p.Val5084Ala
XM_011541108.1:c.15404T>C	XP_011539410.1:p.Val5135Ala
XM_011541109.1:c.15401T>C	XP_011539411.1:p.Val5134Ala
XM_011541110.1:c.15401T>C	XP_011539412.1:p.Val5134Ala
XM_011541111.1:c.15401T>C	XP_011539413.1:p.Val5134Ala
XM_011541112.1:c.15389T>C	XP_011539414.1:p.Val5130Ala
XM_011541113.1:c.15386T>C	XP_011539415.1:p.Val5129Ala
XM_011541114.1:c.15386T>C	XP_011539416.1:p.Val5129Ala
XM_011541115.1:c.15380T>C	XP_011539417.1:p.Val5127Ala
XM_011541116.1:c.15371T>C	XP_011539418.1:p.Val5124Ala
XM_011541117.1:c.15320T>C	XP_011539419.1:p.Val5107Ala
XM_011541118.1:c.15317T>C	XP_011539420.1:p.Val5106Ala
XM_011541119.1:c.15284T>C	XP_011539421.1:p.Val5095Ala
XM_011541120.1:c.15281T>C	XP_011539422.1:p.Val5094Ala
XM_011541121.1:c.15248T>C	XP_011539423.1:p.Val5083Ala
XM_011541108.3:c.15518T>C	XP_011539410.2:p.Val5173Ala
XM_011541109.3:c.15515T>C	XP_011539411.2:p.Val5172Ala
XM_011541110.3:c.15515T>C	XP_011539412.2:p.Val5172Ala
XM_011541111.3:c.15515T>C	XP_011539413.2:p.Val5172Ala
XM_011541112.3:c.15503T>C	XP_011539414.2:p.Val5168Ala
XM_011541113.3:c.15500T>C	XP_011539415.2:p.Val5167Ala
XM_011541114.3:c.15500T>C	XP_011539416.2:p.Val5167Ala
XM_011541115.3:c.15494T>C	XP_011539417.2:p.Val5165Ala
XM_011541116.3:c.15485T>C	XP_011539418.2:p.Val5162Ala
XM_011541117.3:c.15434T>C	XP_011539419.2:p.Val5145Ala
XM_011541118.3:c.15431T>C	XP_011539420.2:p.Val5144Ala
XM_011541119.3:c.15398T>C	XP_011539421.2:p.Val5133Ala
XM_011541120.3:c.15395T>C	XP_011539422.2:p.Val5132Ala
XM_011541121.3:c.15362T>C	XP_011539423.2:p.Val5121Ala
XM_017000822.2:c.15497T>C	XP_016856311.2:p.Val5166Ala
XM_017000823.2:c.15470T>C	XP_016856312.2:p.Val5157Ala
XM_017000824.2:c.15416T>C	XP_016856313.2:p.Val5139Ala
XM_017000825.2:c.15401T>C	XP_016856314.2:p.Val5134Ala
XM_017000826.2:c.15398T>C	XP_016856315.2:p.Val5133Ala
XM_017000827.2:c.15383T>C	XP_016856316.2:p.Val5128Ala
XM_017000828.2:c.15359T>C	XP_016856317.2:p.Val5120Ala
XM_017000829.2:c.15311T>C	XP_016856318.2:p.Val5104Ala
XM_017000830.2:c.15260T>C	XP_016856319.2:p.Val5087Ala
NM_020765.3:c.15251T>C MANE Select	NP_065816.2:p.Val5084Ala