Canonical Allele Identifier: CA1156955993
Gene: UBR4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077819_19077820delinsAT , CM000663.2:g.19077819_19077820delinsAT GRCh38
NC_000001.10:g.19404313_19404314delinsAT , CM000663.1:g.19404313_19404314delinsAT GRCh37
NC_000001.9:g.19276900_19276901delinsAT NCBI36
NG_027669.1:g.137433_137434delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+156_15324+157delinsAT MANE Select ENSP00000364403.3:n.15324+156_15324+157delinsAT
ENST00000375224.1:c.2445+156_2445+157delinsAT ENSP00000364372.1:n.2445+156_2445+157delinsAT
ENST00000375225.7:c.549+156_549+157delinsAT ENSP00000364373.3:n.549+156_549+157delinsAT
ENST00000375254.7:c.15324+156_15324+157delinsAT ENSP00000364403.3:n.15324+156_15324+157delinsAT
ENST00000459947.5:n.3331+156_3331+157delinsAT
ENST00000486515.1:n.8_9delinsAT
NM_020765.2:c.15324+156_15324+157delinsAT NP_065816.2:n.15324+156_15324+157delinsAT
XM_011541108.1:c.15477+156_15477+157delinsAT XP_011539410.1:n.15477+156_15477+157delinsAT
XM_011541109.1:c.15474+156_15474+157delinsAT XP_011539411.1:n.15474+156_15474+157delinsAT
XM_011541110.1:c.15474+156_15474+157delinsAT XP_011539412.1:n.15474+156_15474+157delinsAT
XM_011541111.1:c.15474+156_15474+157delinsAT XP_011539413.1:n.15474+156_15474+157delinsAT
XM_011541112.1:c.15462+156_15462+157delinsAT XP_011539414.1:n.15462+156_15462+157delinsAT
XM_011541113.1:c.15459+156_15459+157delinsAT XP_011539415.1:n.15459+156_15459+157delinsAT
XM_011541114.1:c.15459+156_15459+157delinsAT XP_011539416.1:n.15459+156_15459+157delinsAT
XM_011541115.1:c.15453+156_15453+157delinsAT XP_011539417.1:n.15453+156_15453+157delinsAT
XM_011541116.1:c.15444+156_15444+157delinsAT XP_011539418.1:n.15444+156_15444+157delinsAT
XM_011541117.1:c.15393+156_15393+157delinsAT XP_011539419.1:n.15393+156_15393+157delinsAT
XM_011541118.1:c.15390+156_15390+157delinsAT XP_011539420.1:n.15390+156_15390+157delinsAT
XM_011541119.1:c.15357+156_15357+157delinsAT XP_011539421.1:n.15357+156_15357+157delinsAT
XM_011541120.1:c.15354+156_15354+157delinsAT XP_011539422.1:n.15354+156_15354+157delinsAT
XM_011541121.1:c.15321+156_15321+157delinsAT XP_011539423.1:n.15321+156_15321+157delinsAT
XM_011541108.3:c.15591+156_15591+157delinsAT XP_011539410.2:n.15591+156_15591+157delinsAT
XM_011541109.3:c.15588+156_15588+157delinsAT XP_011539411.2:n.15588+156_15588+157delinsAT
XM_011541110.3:c.15588+156_15588+157delinsAT XP_011539412.2:n.15588+156_15588+157delinsAT
XM_011541111.3:c.15588+156_15588+157delinsAT XP_011539413.2:n.15588+156_15588+157delinsAT
XM_011541112.3:c.15576+156_15576+157delinsAT XP_011539414.2:n.15576+156_15576+157delinsAT
XM_011541113.3:c.15573+156_15573+157delinsAT XP_011539415.2:n.15573+156_15573+157delinsAT
XM_011541114.3:c.15573+156_15573+157delinsAT XP_011539416.2:n.15573+156_15573+157delinsAT
XM_011541115.3:c.15567+156_15567+157delinsAT XP_011539417.2:n.15567+156_15567+157delinsAT
XM_011541116.3:c.15558+156_15558+157delinsAT XP_011539418.2:n.15558+156_15558+157delinsAT
XM_011541117.3:c.15507+156_15507+157delinsAT XP_011539419.2:n.15507+156_15507+157delinsAT
XM_011541118.3:c.15504+156_15504+157delinsAT XP_011539420.2:n.15504+156_15504+157delinsAT
XM_011541119.3:c.15471+156_15471+157delinsAT XP_011539421.2:n.15471+156_15471+157delinsAT
XM_011541120.3:c.15468+156_15468+157delinsAT XP_011539422.2:n.15468+156_15468+157delinsAT
XM_011541121.3:c.15435+156_15435+157delinsAT XP_011539423.2:n.15435+156_15435+157delinsAT
XM_017000822.2:c.15570+156_15570+157delinsAT XP_016856311.2:n.15570+156_15570+157delinsAT
XM_017000823.2:c.15543+156_15543+157delinsAT XP_016856312.2:n.15543+156_15543+157delinsAT
XM_017000824.2:c.15489+156_15489+157delinsAT XP_016856313.2:n.15489+156_15489+157delinsAT
XM_017000825.2:c.15474+156_15474+157delinsAT XP_016856314.2:n.15474+156_15474+157delinsAT
XM_017000826.2:c.15471+156_15471+157delinsAT XP_016856315.2:n.15471+156_15471+157delinsAT
XM_017000827.2:c.15456+156_15456+157delinsAT XP_016856316.2:n.15456+156_15456+157delinsAT
XM_017000828.2:c.15432+156_15432+157delinsAT XP_016856317.2:n.15432+156_15432+157delinsAT
XM_017000829.2:c.15384+156_15384+157delinsAT XP_016856318.2:n.15384+156_15384+157delinsAT
XM_017000830.2:c.15333+156_15333+157delinsAT XP_016856319.2:n.15333+156_15333+157delinsAT
NM_020765.3:c.15324+156_15324+157delinsAT MANE Select NP_065816.2:n.15324+156_15324+157delinsAT
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