Canonical Allele Identifier: CA1156956036
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077910_19077911delinsAG , CM000663.2:g.19077910_19077911delinsAG GRCh38
NC_000001.10:g.19404404_19404405delinsAG , CM000663.1:g.19404404_19404405delinsAG GRCh37
NC_000001.9:g.19276991_19276992delinsAG NCBI36
NG_027669.1:g.137342_137343delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+65_15324+66delinsCT MANE Select ENSP00000364403.3:n.15324+65_15324+66delinsCT
ENST00000375224.1:c.2445+65_2445+66delinsCT ENSP00000364372.1:n.2445+65_2445+66delinsCT
ENST00000375225.7:c.549+65_549+66delinsCT ENSP00000364373.3:n.549+65_549+66delinsCT
ENST00000375254.7:c.15324+65_15324+66delinsCT ENSP00000364403.3:n.15324+65_15324+66delinsCT
ENST00000459947.5:n.3331+65_3331+66delinsCT
NM_020765.2:c.15324+65_15324+66delinsCT NP_065816.2:n.15324+65_15324+66delinsCT
XM_011541108.1:c.15477+65_15477+66delinsCT XP_011539410.1:n.15477+65_15477+66delinsCT
XM_011541109.1:c.15474+65_15474+66delinsCT XP_011539411.1:n.15474+65_15474+66delinsCT
XM_011541110.1:c.15474+65_15474+66delinsCT XP_011539412.1:n.15474+65_15474+66delinsCT
XM_011541111.1:c.15474+65_15474+66delinsCT XP_011539413.1:n.15474+65_15474+66delinsCT
XM_011541112.1:c.15462+65_15462+66delinsCT XP_011539414.1:n.15462+65_15462+66delinsCT
XM_011541113.1:c.15459+65_15459+66delinsCT XP_011539415.1:n.15459+65_15459+66delinsCT
XM_011541114.1:c.15459+65_15459+66delinsCT XP_011539416.1:n.15459+65_15459+66delinsCT
XM_011541115.1:c.15453+65_15453+66delinsCT XP_011539417.1:n.15453+65_15453+66delinsCT
XM_011541116.1:c.15444+65_15444+66delinsCT XP_011539418.1:n.15444+65_15444+66delinsCT
XM_011541117.1:c.15393+65_15393+66delinsCT XP_011539419.1:n.15393+65_15393+66delinsCT
XM_011541118.1:c.15390+65_15390+66delinsCT XP_011539420.1:n.15390+65_15390+66delinsCT
XM_011541119.1:c.15357+65_15357+66delinsCT XP_011539421.1:n.15357+65_15357+66delinsCT
XM_011541120.1:c.15354+65_15354+66delinsCT XP_011539422.1:n.15354+65_15354+66delinsCT
XM_011541121.1:c.15321+65_15321+66delinsCT XP_011539423.1:n.15321+65_15321+66delinsCT
XM_011541108.3:c.15591+65_15591+66delinsCT XP_011539410.2:n.15591+65_15591+66delinsCT
XM_011541109.3:c.15588+65_15588+66delinsCT XP_011539411.2:n.15588+65_15588+66delinsCT
XM_011541110.3:c.15588+65_15588+66delinsCT XP_011539412.2:n.15588+65_15588+66delinsCT
XM_011541111.3:c.15588+65_15588+66delinsCT XP_011539413.2:n.15588+65_15588+66delinsCT
XM_011541112.3:c.15576+65_15576+66delinsCT XP_011539414.2:n.15576+65_15576+66delinsCT
XM_011541113.3:c.15573+65_15573+66delinsCT XP_011539415.2:n.15573+65_15573+66delinsCT
XM_011541114.3:c.15573+65_15573+66delinsCT XP_011539416.2:n.15573+65_15573+66delinsCT
XM_011541115.3:c.15567+65_15567+66delinsCT XP_011539417.2:n.15567+65_15567+66delinsCT
XM_011541116.3:c.15558+65_15558+66delinsCT XP_011539418.2:n.15558+65_15558+66delinsCT
XM_011541117.3:c.15507+65_15507+66delinsCT XP_011539419.2:n.15507+65_15507+66delinsCT
XM_011541118.3:c.15504+65_15504+66delinsCT XP_011539420.2:n.15504+65_15504+66delinsCT
XM_011541119.3:c.15471+65_15471+66delinsCT XP_011539421.2:n.15471+65_15471+66delinsCT
XM_011541120.3:c.15468+65_15468+66delinsCT XP_011539422.2:n.15468+65_15468+66delinsCT
XM_011541121.3:c.15435+65_15435+66delinsCT XP_011539423.2:n.15435+65_15435+66delinsCT
XM_017000822.2:c.15570+65_15570+66delinsCT XP_016856311.2:n.15570+65_15570+66delinsCT
XM_017000823.2:c.15543+65_15543+66delinsCT XP_016856312.2:n.15543+65_15543+66delinsCT
XM_017000824.2:c.15489+65_15489+66delinsCT XP_016856313.2:n.15489+65_15489+66delinsCT
XM_017000825.2:c.15474+65_15474+66delinsCT XP_016856314.2:n.15474+65_15474+66delinsCT
XM_017000826.2:c.15471+65_15471+66delinsCT XP_016856315.2:n.15471+65_15471+66delinsCT
XM_017000827.2:c.15456+65_15456+66delinsCT XP_016856316.2:n.15456+65_15456+66delinsCT
XM_017000828.2:c.15432+65_15432+66delinsCT XP_016856317.2:n.15432+65_15432+66delinsCT
XM_017000829.2:c.15384+65_15384+66delinsCT XP_016856318.2:n.15384+65_15384+66delinsCT
XM_017000830.2:c.15333+65_15333+66delinsCT XP_016856319.2:n.15333+65_15333+66delinsCT
NM_020765.3:c.15324+65_15324+66delinsCT MANE Select NP_065816.2:n.15324+65_15324+66delinsCT