Canonical Allele Identifier: CA338748195
Gene: UBR4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15277T>G MANE Select ENSP00000364403.3:p.Ser5093Ala
ENST00000375224.1:c.2398T>G ENSP00000364372.1:p.Ser800Ala
ENST00000375225.7:c.502T>G ENSP00000364373.3:p.Ser168Ala
ENST00000375254.7:c.15277T>G ENSP00000364403.3:p.Ser5093Ala
ENST00000459947.5:n.3284T>G
NM_020765.2:c.15277T>G NP_065816.2:p.Ser5093Ala
XM_011541108.1:c.15430T>G XP_011539410.1:p.Ser5144Ala
XM_011541109.1:c.15427T>G XP_011539411.1:p.Ser5143Ala
XM_011541110.1:c.15427T>G XP_011539412.1:p.Ser5143Ala
XM_011541111.1:c.15427T>G XP_011539413.1:p.Ser5143Ala
XM_011541112.1:c.15415T>G XP_011539414.1:p.Ser5139Ala
XM_011541113.1:c.15412T>G XP_011539415.1:p.Ser5138Ala
XM_011541114.1:c.15412T>G XP_011539416.1:p.Ser5138Ala
XM_011541115.1:c.15406T>G XP_011539417.1:p.Ser5136Ala
XM_011541116.1:c.15397T>G XP_011539418.1:p.Ser5133Ala
XM_011541117.1:c.15346T>G XP_011539419.1:p.Ser5116Ala
XM_011541118.1:c.15343T>G XP_011539420.1:p.Ser5115Ala
XM_011541119.1:c.15310T>G XP_011539421.1:p.Ser5104Ala
XM_011541120.1:c.15307T>G XP_011539422.1:p.Ser5103Ala
XM_011541121.1:c.15274T>G XP_011539423.1:p.Ser5092Ala
XM_011541108.3:c.15544T>G XP_011539410.2:p.Ser5182Ala
XM_011541109.3:c.15541T>G XP_011539411.2:p.Ser5181Ala
XM_011541110.3:c.15541T>G XP_011539412.2:p.Ser5181Ala
XM_011541111.3:c.15541T>G XP_011539413.2:p.Ser5181Ala
XM_011541112.3:c.15529T>G XP_011539414.2:p.Ser5177Ala
XM_011541113.3:c.15526T>G XP_011539415.2:p.Ser5176Ala
XM_011541114.3:c.15526T>G XP_011539416.2:p.Ser5176Ala
XM_011541115.3:c.15520T>G XP_011539417.2:p.Ser5174Ala
XM_011541116.3:c.15511T>G XP_011539418.2:p.Ser5171Ala
XM_011541117.3:c.15460T>G XP_011539419.2:p.Ser5154Ala
XM_011541118.3:c.15457T>G XP_011539420.2:p.Ser5153Ala
XM_011541119.3:c.15424T>G XP_011539421.2:p.Ser5142Ala
XM_011541120.3:c.15421T>G XP_011539422.2:p.Ser5141Ala
XM_011541121.3:c.15388T>G XP_011539423.2:p.Ser5130Ala
XM_017000822.2:c.15523T>G XP_016856311.2:p.Ser5175Ala
XM_017000823.2:c.15496T>G XP_016856312.2:p.Ser5166Ala
XM_017000824.2:c.15442T>G XP_016856313.2:p.Ser5148Ala
XM_017000825.2:c.15427T>G XP_016856314.2:p.Ser5143Ala
XM_017000826.2:c.15424T>G XP_016856315.2:p.Ser5142Ala
XM_017000827.2:c.15409T>G XP_016856316.2:p.Ser5137Ala
XM_017000828.2:c.15385T>G XP_016856317.2:p.Ser5129Ala
XM_017000829.2:c.15337T>G XP_016856318.2:p.Ser5113Ala
XM_017000830.2:c.15286T>G XP_016856319.2:p.Ser5096Ala
NM_020765.3:c.15277T>G MANE Select NP_065816.2:p.Ser5093Ala