Canonical Allele Identifier: CA338748358

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404559G>T (hg19) ; chr1:g.19078065G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078065G>T , CM000663.2:g.19078065G>T	GRCh38
NC_000001.10:g.19404559G>T , CM000663.1:g.19404559G>T	GRCh37
NC_000001.9:g.19277146G>T	NCBI36
NG_027669.1:g.137188C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15235C>A MANE Select	ENSP00000364403.3:p.Leu5079Met
ENST00000375224.1:c.2356C>A	ENSP00000364372.1:p.Leu786Met
ENST00000375225.7:c.460C>A	ENSP00000364373.3:p.Leu154Met
ENST00000375254.7:c.15235C>A	ENSP00000364403.3:p.Leu5079Met
ENST00000459947.5:n.3242C>A
NM_020765.2:c.15235C>A	NP_065816.2:p.Leu5079Met
XM_011541108.1:c.15388C>A	XP_011539410.1:p.Leu5130Met
XM_011541109.1:c.15385C>A	XP_011539411.1:p.Leu5129Met
XM_011541110.1:c.15385C>A	XP_011539412.1:p.Leu5129Met
XM_011541111.1:c.15385C>A	XP_011539413.1:p.Leu5129Met
XM_011541112.1:c.15373C>A	XP_011539414.1:p.Leu5125Met
XM_011541113.1:c.15370C>A	XP_011539415.1:p.Leu5124Met
XM_011541114.1:c.15370C>A	XP_011539416.1:p.Leu5124Met
XM_011541115.1:c.15364C>A	XP_011539417.1:p.Leu5122Met
XM_011541116.1:c.15355C>A	XP_011539418.1:p.Leu5119Met
XM_011541117.1:c.15304C>A	XP_011539419.1:p.Leu5102Met
XM_011541118.1:c.15301C>A	XP_011539420.1:p.Leu5101Met
XM_011541119.1:c.15268C>A	XP_011539421.1:p.Leu5090Met
XM_011541120.1:c.15265C>A	XP_011539422.1:p.Leu5089Met
XM_011541121.1:c.15232C>A	XP_011539423.1:p.Leu5078Met
XM_011541108.3:c.15502C>A	XP_011539410.2:p.Leu5168Met
XM_011541109.3:c.15499C>A	XP_011539411.2:p.Leu5167Met
XM_011541110.3:c.15499C>A	XP_011539412.2:p.Leu5167Met
XM_011541111.3:c.15499C>A	XP_011539413.2:p.Leu5167Met
XM_011541112.3:c.15487C>A	XP_011539414.2:p.Leu5163Met
XM_011541113.3:c.15484C>A	XP_011539415.2:p.Leu5162Met
XM_011541114.3:c.15484C>A	XP_011539416.2:p.Leu5162Met
XM_011541115.3:c.15478C>A	XP_011539417.2:p.Leu5160Met
XM_011541116.3:c.15469C>A	XP_011539418.2:p.Leu5157Met
XM_011541117.3:c.15418C>A	XP_011539419.2:p.Leu5140Met
XM_011541118.3:c.15415C>A	XP_011539420.2:p.Leu5139Met
XM_011541119.3:c.15382C>A	XP_011539421.2:p.Leu5128Met
XM_011541120.3:c.15379C>A	XP_011539422.2:p.Leu5127Met
XM_011541121.3:c.15346C>A	XP_011539423.2:p.Leu5116Met
XM_017000822.2:c.15481C>A	XP_016856311.2:p.Leu5161Met
XM_017000823.2:c.15454C>A	XP_016856312.2:p.Leu5152Met
XM_017000824.2:c.15400C>A	XP_016856313.2:p.Leu5134Met
XM_017000825.2:c.15385C>A	XP_016856314.2:p.Leu5129Met
XM_017000826.2:c.15382C>A	XP_016856315.2:p.Leu5128Met
XM_017000827.2:c.15367C>A	XP_016856316.2:p.Leu5123Met
XM_017000828.2:c.15343C>A	XP_016856317.2:p.Leu5115Met
XM_017000829.2:c.15295C>A	XP_016856318.2:p.Leu5099Met
XM_017000830.2:c.15244C>A	XP_016856319.2:p.Leu5082Met
NM_020765.3:c.15235C>A MANE Select	NP_065816.2:p.Leu5079Met