Canonical Allele Identifier: CA1156956034
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077903_19077905delinsCAG , CM000663.2:g.19077903_19077905delinsCAG GRCh38
NC_000001.10:g.19404397_19404399delinsCAG , CM000663.1:g.19404397_19404399delinsCAG GRCh37
NC_000001.9:g.19276984_19276986delinsCAG NCBI36
NG_027669.1:g.137348_137350delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+71_15324+73delinsCTG MANE Select ENSP00000364403.3:n.15324+71_15324+73delinsCTG
ENST00000375224.1:c.2445+71_2445+73delinsCTG ENSP00000364372.1:n.2445+71_2445+73delinsCTG
ENST00000375225.7:c.549+71_549+73delinsCTG ENSP00000364373.3:n.549+71_549+73delinsCTG
ENST00000375254.7:c.15324+71_15324+73delinsCTG ENSP00000364403.3:n.15324+71_15324+73delinsCTG
ENST00000459947.5:n.3331+71_3331+73delinsCTG
NM_020765.2:c.15324+71_15324+73delinsCTG NP_065816.2:n.15324+71_15324+73delinsCTG
XM_011541108.1:c.15477+71_15477+73delinsCTG XP_011539410.1:n.15477+71_15477+73delinsCTG
XM_011541109.1:c.15474+71_15474+73delinsCTG XP_011539411.1:n.15474+71_15474+73delinsCTG
XM_011541110.1:c.15474+71_15474+73delinsCTG XP_011539412.1:n.15474+71_15474+73delinsCTG
XM_011541111.1:c.15474+71_15474+73delinsCTG XP_011539413.1:n.15474+71_15474+73delinsCTG
XM_011541112.1:c.15462+71_15462+73delinsCTG XP_011539414.1:n.15462+71_15462+73delinsCTG
XM_011541113.1:c.15459+71_15459+73delinsCTG XP_011539415.1:n.15459+71_15459+73delinsCTG
XM_011541114.1:c.15459+71_15459+73delinsCTG XP_011539416.1:n.15459+71_15459+73delinsCTG
XM_011541115.1:c.15453+71_15453+73delinsCTG XP_011539417.1:n.15453+71_15453+73delinsCTG
XM_011541116.1:c.15444+71_15444+73delinsCTG XP_011539418.1:n.15444+71_15444+73delinsCTG
XM_011541117.1:c.15393+71_15393+73delinsCTG XP_011539419.1:n.15393+71_15393+73delinsCTG
XM_011541118.1:c.15390+71_15390+73delinsCTG XP_011539420.1:n.15390+71_15390+73delinsCTG
XM_011541119.1:c.15357+71_15357+73delinsCTG XP_011539421.1:n.15357+71_15357+73delinsCTG
XM_011541120.1:c.15354+71_15354+73delinsCTG XP_011539422.1:n.15354+71_15354+73delinsCTG
XM_011541121.1:c.15321+71_15321+73delinsCTG XP_011539423.1:n.15321+71_15321+73delinsCTG
XM_011541108.3:c.15591+71_15591+73delinsCTG XP_011539410.2:n.15591+71_15591+73delinsCTG
XM_011541109.3:c.15588+71_15588+73delinsCTG XP_011539411.2:n.15588+71_15588+73delinsCTG
XM_011541110.3:c.15588+71_15588+73delinsCTG XP_011539412.2:n.15588+71_15588+73delinsCTG
XM_011541111.3:c.15588+71_15588+73delinsCTG XP_011539413.2:n.15588+71_15588+73delinsCTG
XM_011541112.3:c.15576+71_15576+73delinsCTG XP_011539414.2:n.15576+71_15576+73delinsCTG
XM_011541113.3:c.15573+71_15573+73delinsCTG XP_011539415.2:n.15573+71_15573+73delinsCTG
XM_011541114.3:c.15573+71_15573+73delinsCTG XP_011539416.2:n.15573+71_15573+73delinsCTG
XM_011541115.3:c.15567+71_15567+73delinsCTG XP_011539417.2:n.15567+71_15567+73delinsCTG
XM_011541116.3:c.15558+71_15558+73delinsCTG XP_011539418.2:n.15558+71_15558+73delinsCTG
XM_011541117.3:c.15507+71_15507+73delinsCTG XP_011539419.2:n.15507+71_15507+73delinsCTG
XM_011541118.3:c.15504+71_15504+73delinsCTG XP_011539420.2:n.15504+71_15504+73delinsCTG
XM_011541119.3:c.15471+71_15471+73delinsCTG XP_011539421.2:n.15471+71_15471+73delinsCTG
XM_011541120.3:c.15468+71_15468+73delinsCTG XP_011539422.2:n.15468+71_15468+73delinsCTG
XM_011541121.3:c.15435+71_15435+73delinsCTG XP_011539423.2:n.15435+71_15435+73delinsCTG
XM_017000822.2:c.15570+71_15570+73delinsCTG XP_016856311.2:n.15570+71_15570+73delinsCTG
XM_017000823.2:c.15543+71_15543+73delinsCTG XP_016856312.2:n.15543+71_15543+73delinsCTG
XM_017000824.2:c.15489+71_15489+73delinsCTG XP_016856313.2:n.15489+71_15489+73delinsCTG
XM_017000825.2:c.15474+71_15474+73delinsCTG XP_016856314.2:n.15474+71_15474+73delinsCTG
XM_017000826.2:c.15471+71_15471+73delinsCTG XP_016856315.2:n.15471+71_15471+73delinsCTG
XM_017000827.2:c.15456+71_15456+73delinsCTG XP_016856316.2:n.15456+71_15456+73delinsCTG
XM_017000828.2:c.15432+71_15432+73delinsCTG XP_016856317.2:n.15432+71_15432+73delinsCTG
XM_017000829.2:c.15384+71_15384+73delinsCTG XP_016856318.2:n.15384+71_15384+73delinsCTG
XM_017000830.2:c.15333+71_15333+73delinsCTG XP_016856319.2:n.15333+71_15333+73delinsCTG
NM_020765.3:c.15324+71_15324+73delinsCTG MANE Select NP_065816.2:n.15324+71_15324+73delinsCTG