Canonical Allele Identifier: CA338748102
Gene: UBR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077992A>C , CM000663.2:g.19077992A>C GRCh38
NC_000001.10:g.19404486A>C , CM000663.1:g.19404486A>C GRCh37
NC_000001.9:g.19277073A>C NCBI36
NG_027669.1:g.137261T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15308T>G MANE Select ENSP00000364403.3:p.Ile5103Ser
ENST00000375224.1:c.2429T>G ENSP00000364372.1:p.Ile810Ser
ENST00000375225.7:c.533T>G ENSP00000364373.3:p.Ile178Ser
ENST00000375254.7:c.15308T>G ENSP00000364403.3:p.Ile5103Ser
ENST00000459947.5:n.3315T>G
NM_020765.2:c.15308T>G NP_065816.2:p.Ile5103Ser
XM_011541108.1:c.15461T>G XP_011539410.1:p.Ile5154Ser
XM_011541109.1:c.15458T>G XP_011539411.1:p.Ile5153Ser
XM_011541110.1:c.15458T>G XP_011539412.1:p.Ile5153Ser
XM_011541111.1:c.15458T>G XP_011539413.1:p.Ile5153Ser
XM_011541112.1:c.15446T>G XP_011539414.1:p.Ile5149Ser
XM_011541113.1:c.15443T>G XP_011539415.1:p.Ile5148Ser
XM_011541114.1:c.15443T>G XP_011539416.1:p.Ile5148Ser
XM_011541115.1:c.15437T>G XP_011539417.1:p.Ile5146Ser
XM_011541116.1:c.15428T>G XP_011539418.1:p.Ile5143Ser
XM_011541117.1:c.15377T>G XP_011539419.1:p.Ile5126Ser
XM_011541118.1:c.15374T>G XP_011539420.1:p.Ile5125Ser
XM_011541119.1:c.15341T>G XP_011539421.1:p.Ile5114Ser
XM_011541120.1:c.15338T>G XP_011539422.1:p.Ile5113Ser
XM_011541121.1:c.15305T>G XP_011539423.1:p.Ile5102Ser
XM_011541108.3:c.15575T>G XP_011539410.2:p.Ile5192Ser
XM_011541109.3:c.15572T>G XP_011539411.2:p.Ile5191Ser
XM_011541110.3:c.15572T>G XP_011539412.2:p.Ile5191Ser
XM_011541111.3:c.15572T>G XP_011539413.2:p.Ile5191Ser
XM_011541112.3:c.15560T>G XP_011539414.2:p.Ile5187Ser
XM_011541113.3:c.15557T>G XP_011539415.2:p.Ile5186Ser
XM_011541114.3:c.15557T>G XP_011539416.2:p.Ile5186Ser
XM_011541115.3:c.15551T>G XP_011539417.2:p.Ile5184Ser
XM_011541116.3:c.15542T>G XP_011539418.2:p.Ile5181Ser
XM_011541117.3:c.15491T>G XP_011539419.2:p.Ile5164Ser
XM_011541118.3:c.15488T>G XP_011539420.2:p.Ile5163Ser
XM_011541119.3:c.15455T>G XP_011539421.2:p.Ile5152Ser
XM_011541120.3:c.15452T>G XP_011539422.2:p.Ile5151Ser
XM_011541121.3:c.15419T>G XP_011539423.2:p.Ile5140Ser
XM_017000822.2:c.15554T>G XP_016856311.2:p.Ile5185Ser
XM_017000823.2:c.15527T>G XP_016856312.2:p.Ile5176Ser
XM_017000824.2:c.15473T>G XP_016856313.2:p.Ile5158Ser
XM_017000825.2:c.15458T>G XP_016856314.2:p.Ile5153Ser
XM_017000826.2:c.15455T>G XP_016856315.2:p.Ile5152Ser
XM_017000827.2:c.15440T>G XP_016856316.2:p.Ile5147Ser
XM_017000828.2:c.15416T>G XP_016856317.2:p.Ile5139Ser
XM_017000829.2:c.15368T>G XP_016856318.2:p.Ile5123Ser
XM_017000830.2:c.15317T>G XP_016856319.2:p.Ile5106Ser
NM_020765.3:c.15308T>G MANE Select NP_065816.2:p.Ile5103Ser