Canonical Allele Identifier: CA338748198

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404517A>T (hg19) ; chr1:g.19078023A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078023A>T , CM000663.2:g.19078023A>T	GRCh38
NC_000001.10:g.19404517A>T , CM000663.1:g.19404517A>T	GRCh37
NC_000001.9:g.19277104A>T	NCBI36
NG_027669.1:g.137230T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15277T>A MANE Select	ENSP00000364403.3:p.Ser5093Thr
ENST00000375224.1:c.2398T>A	ENSP00000364372.1:p.Ser800Thr
ENST00000375225.7:c.502T>A	ENSP00000364373.3:p.Ser168Thr
ENST00000375254.7:c.15277T>A	ENSP00000364403.3:p.Ser5093Thr
ENST00000459947.5:n.3284T>A
NM_020765.2:c.15277T>A	NP_065816.2:p.Ser5093Thr
XM_011541108.1:c.15430T>A	XP_011539410.1:p.Ser5144Thr
XM_011541109.1:c.15427T>A	XP_011539411.1:p.Ser5143Thr
XM_011541110.1:c.15427T>A	XP_011539412.1:p.Ser5143Thr
XM_011541111.1:c.15427T>A	XP_011539413.1:p.Ser5143Thr
XM_011541112.1:c.15415T>A	XP_011539414.1:p.Ser5139Thr
XM_011541113.1:c.15412T>A	XP_011539415.1:p.Ser5138Thr
XM_011541114.1:c.15412T>A	XP_011539416.1:p.Ser5138Thr
XM_011541115.1:c.15406T>A	XP_011539417.1:p.Ser5136Thr
XM_011541116.1:c.15397T>A	XP_011539418.1:p.Ser5133Thr
XM_011541117.1:c.15346T>A	XP_011539419.1:p.Ser5116Thr
XM_011541118.1:c.15343T>A	XP_011539420.1:p.Ser5115Thr
XM_011541119.1:c.15310T>A	XP_011539421.1:p.Ser5104Thr
XM_011541120.1:c.15307T>A	XP_011539422.1:p.Ser5103Thr
XM_011541121.1:c.15274T>A	XP_011539423.1:p.Ser5092Thr
XM_011541108.3:c.15544T>A	XP_011539410.2:p.Ser5182Thr
XM_011541109.3:c.15541T>A	XP_011539411.2:p.Ser5181Thr
XM_011541110.3:c.15541T>A	XP_011539412.2:p.Ser5181Thr
XM_011541111.3:c.15541T>A	XP_011539413.2:p.Ser5181Thr
XM_011541112.3:c.15529T>A	XP_011539414.2:p.Ser5177Thr
XM_011541113.3:c.15526T>A	XP_011539415.2:p.Ser5176Thr
XM_011541114.3:c.15526T>A	XP_011539416.2:p.Ser5176Thr
XM_011541115.3:c.15520T>A	XP_011539417.2:p.Ser5174Thr
XM_011541116.3:c.15511T>A	XP_011539418.2:p.Ser5171Thr
XM_011541117.3:c.15460T>A	XP_011539419.2:p.Ser5154Thr
XM_011541118.3:c.15457T>A	XP_011539420.2:p.Ser5153Thr
XM_011541119.3:c.15424T>A	XP_011539421.2:p.Ser5142Thr
XM_011541120.3:c.15421T>A	XP_011539422.2:p.Ser5141Thr
XM_011541121.3:c.15388T>A	XP_011539423.2:p.Ser5130Thr
XM_017000822.2:c.15523T>A	XP_016856311.2:p.Ser5175Thr
XM_017000823.2:c.15496T>A	XP_016856312.2:p.Ser5166Thr
XM_017000824.2:c.15442T>A	XP_016856313.2:p.Ser5148Thr
XM_017000825.2:c.15427T>A	XP_016856314.2:p.Ser5143Thr
XM_017000826.2:c.15424T>A	XP_016856315.2:p.Ser5142Thr
XM_017000827.2:c.15409T>A	XP_016856316.2:p.Ser5137Thr
XM_017000828.2:c.15385T>A	XP_016856317.2:p.Ser5129Thr
XM_017000829.2:c.15337T>A	XP_016856318.2:p.Ser5113Thr
XM_017000830.2:c.15286T>A	XP_016856319.2:p.Ser5096Thr
NM_020765.3:c.15277T>A MANE Select	NP_065816.2:p.Ser5093Thr