Canonical Allele Identifier: CA1156956052
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077947_19077948delinsAC , CM000663.2:g.19077947_19077948delinsAC GRCh38
NC_000001.10:g.19404441_19404442delinsAC , CM000663.1:g.19404441_19404442delinsAC GRCh37
NC_000001.9:g.19277028_19277029delinsAC NCBI36
NG_027669.1:g.137305_137306delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+28_15324+29delinsGT MANE Select ENSP00000364403.3:n.15324+28_15324+29delinsGT
ENST00000375224.1:c.2445+28_2445+29delinsGT ENSP00000364372.1:n.2445+28_2445+29delinsGT
ENST00000375225.7:c.549+28_549+29delinsGT ENSP00000364373.3:n.549+28_549+29delinsGT
ENST00000375254.7:c.15324+28_15324+29delinsGT ENSP00000364403.3:n.15324+28_15324+29delinsGT
ENST00000459947.5:n.3331+28_3331+29delinsGT
NM_020765.2:c.15324+28_15324+29delinsGT NP_065816.2:n.15324+28_15324+29delinsGT
XM_011541108.1:c.15477+28_15477+29delinsGT XP_011539410.1:n.15477+28_15477+29delinsGT
XM_011541109.1:c.15474+28_15474+29delinsGT XP_011539411.1:n.15474+28_15474+29delinsGT
XM_011541110.1:c.15474+28_15474+29delinsGT XP_011539412.1:n.15474+28_15474+29delinsGT
XM_011541111.1:c.15474+28_15474+29delinsGT XP_011539413.1:n.15474+28_15474+29delinsGT
XM_011541112.1:c.15462+28_15462+29delinsGT XP_011539414.1:n.15462+28_15462+29delinsGT
XM_011541113.1:c.15459+28_15459+29delinsGT XP_011539415.1:n.15459+28_15459+29delinsGT
XM_011541114.1:c.15459+28_15459+29delinsGT XP_011539416.1:n.15459+28_15459+29delinsGT
XM_011541115.1:c.15453+28_15453+29delinsGT XP_011539417.1:n.15453+28_15453+29delinsGT
XM_011541116.1:c.15444+28_15444+29delinsGT XP_011539418.1:n.15444+28_15444+29delinsGT
XM_011541117.1:c.15393+28_15393+29delinsGT XP_011539419.1:n.15393+28_15393+29delinsGT
XM_011541118.1:c.15390+28_15390+29delinsGT XP_011539420.1:n.15390+28_15390+29delinsGT
XM_011541119.1:c.15357+28_15357+29delinsGT XP_011539421.1:n.15357+28_15357+29delinsGT
XM_011541120.1:c.15354+28_15354+29delinsGT XP_011539422.1:n.15354+28_15354+29delinsGT
XM_011541121.1:c.15321+28_15321+29delinsGT XP_011539423.1:n.15321+28_15321+29delinsGT
XM_011541108.3:c.15591+28_15591+29delinsGT XP_011539410.2:n.15591+28_15591+29delinsGT
XM_011541109.3:c.15588+28_15588+29delinsGT XP_011539411.2:n.15588+28_15588+29delinsGT
XM_011541110.3:c.15588+28_15588+29delinsGT XP_011539412.2:n.15588+28_15588+29delinsGT
XM_011541111.3:c.15588+28_15588+29delinsGT XP_011539413.2:n.15588+28_15588+29delinsGT
XM_011541112.3:c.15576+28_15576+29delinsGT XP_011539414.2:n.15576+28_15576+29delinsGT
XM_011541113.3:c.15573+28_15573+29delinsGT XP_011539415.2:n.15573+28_15573+29delinsGT
XM_011541114.3:c.15573+28_15573+29delinsGT XP_011539416.2:n.15573+28_15573+29delinsGT
XM_011541115.3:c.15567+28_15567+29delinsGT XP_011539417.2:n.15567+28_15567+29delinsGT
XM_011541116.3:c.15558+28_15558+29delinsGT XP_011539418.2:n.15558+28_15558+29delinsGT
XM_011541117.3:c.15507+28_15507+29delinsGT XP_011539419.2:n.15507+28_15507+29delinsGT
XM_011541118.3:c.15504+28_15504+29delinsGT XP_011539420.2:n.15504+28_15504+29delinsGT
XM_011541119.3:c.15471+28_15471+29delinsGT XP_011539421.2:n.15471+28_15471+29delinsGT
XM_011541120.3:c.15468+28_15468+29delinsGT XP_011539422.2:n.15468+28_15468+29delinsGT
XM_011541121.3:c.15435+28_15435+29delinsGT XP_011539423.2:n.15435+28_15435+29delinsGT
XM_017000822.2:c.15570+28_15570+29delinsGT XP_016856311.2:n.15570+28_15570+29delinsGT
XM_017000823.2:c.15543+28_15543+29delinsGT XP_016856312.2:n.15543+28_15543+29delinsGT
XM_017000824.2:c.15489+28_15489+29delinsGT XP_016856313.2:n.15489+28_15489+29delinsGT
XM_017000825.2:c.15474+28_15474+29delinsGT XP_016856314.2:n.15474+28_15474+29delinsGT
XM_017000826.2:c.15471+28_15471+29delinsGT XP_016856315.2:n.15471+28_15471+29delinsGT
XM_017000827.2:c.15456+28_15456+29delinsGT XP_016856316.2:n.15456+28_15456+29delinsGT
XM_017000828.2:c.15432+28_15432+29delinsGT XP_016856317.2:n.15432+28_15432+29delinsGT
XM_017000829.2:c.15384+28_15384+29delinsGT XP_016856318.2:n.15384+28_15384+29delinsGT
XM_017000830.2:c.15333+28_15333+29delinsGT XP_016856319.2:n.15333+28_15333+29delinsGT
NM_020765.3:c.15324+28_15324+29delinsGT MANE Select NP_065816.2:n.15324+28_15324+29delinsGT