Canonical Allele Identifier: CA999227652
Gene: UBR4 HGNC NCBI

Linked Data

dbSNP Id: rs2076104568

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077858del , CM000663.2:g.19077858del GRCh38
NC_000001.10:g.19404352del , CM000663.1:g.19404352del GRCh37
NC_000001.9:g.19276939del NCBI36
NG_027669.1:g.137400del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+123del MANE Select ENSP00000364403.3:n.15324+123del
ENST00000375224.1:c.2445+123del ENSP00000364372.1:n.2445+123del
ENST00000375225.7:c.549+123del ENSP00000364373.3:n.549+123del
ENST00000375254.7:c.15324+123del ENSP00000364403.3:n.15324+123del
ENST00000459947.5:n.3331+123del
NM_020765.2:c.15324+123del NP_065816.2:n.15324+123del
XM_011541108.1:c.15477+123del XP_011539410.1:n.15477+123del
XM_011541109.1:c.15474+123del XP_011539411.1:n.15474+123del
XM_011541110.1:c.15474+123del XP_011539412.1:n.15474+123del
XM_011541111.1:c.15474+123del XP_011539413.1:n.15474+123del
XM_011541112.1:c.15462+123del XP_011539414.1:n.15462+123del
XM_011541113.1:c.15459+123del XP_011539415.1:n.15459+123del
XM_011541114.1:c.15459+123del XP_011539416.1:n.15459+123del
XM_011541115.1:c.15453+123del XP_011539417.1:n.15453+123del
XM_011541116.1:c.15444+123del XP_011539418.1:n.15444+123del
XM_011541117.1:c.15393+123del XP_011539419.1:n.15393+123del
XM_011541118.1:c.15390+123del XP_011539420.1:n.15390+123del
XM_011541119.1:c.15357+123del XP_011539421.1:n.15357+123del
XM_011541120.1:c.15354+123del XP_011539422.1:n.15354+123del
XM_011541121.1:c.15321+123del XP_011539423.1:n.15321+123del
XM_011541108.3:c.15591+123del XP_011539410.2:n.15591+123del
XM_011541109.3:c.15588+123del XP_011539411.2:n.15588+123del
XM_011541110.3:c.15588+123del XP_011539412.2:n.15588+123del
XM_011541111.3:c.15588+123del XP_011539413.2:n.15588+123del
XM_011541112.3:c.15576+123del XP_011539414.2:n.15576+123del
XM_011541113.3:c.15573+123del XP_011539415.2:n.15573+123del
XM_011541114.3:c.15573+123del XP_011539416.2:n.15573+123del
XM_011541115.3:c.15567+123del XP_011539417.2:n.15567+123del
XM_011541116.3:c.15558+123del XP_011539418.2:n.15558+123del
XM_011541117.3:c.15507+123del XP_011539419.2:n.15507+123del
XM_011541118.3:c.15504+123del XP_011539420.2:n.15504+123del
XM_011541119.3:c.15471+123del XP_011539421.2:n.15471+123del
XM_011541120.3:c.15468+123del XP_011539422.2:n.15468+123del
XM_011541121.3:c.15435+123del XP_011539423.2:n.15435+123del
XM_017000822.2:c.15570+123del XP_016856311.2:n.15570+123del
XM_017000823.2:c.15543+123del XP_016856312.2:n.15543+123del
XM_017000824.2:c.15489+123del XP_016856313.2:n.15489+123del
XM_017000825.2:c.15474+123del XP_016856314.2:n.15474+123del
XM_017000826.2:c.15471+123del XP_016856315.2:n.15471+123del
XM_017000827.2:c.15456+123del XP_016856316.2:n.15456+123del
XM_017000828.2:c.15432+123del XP_016856317.2:n.15432+123del
XM_017000829.2:c.15384+123del XP_016856318.2:n.15384+123del
XM_017000830.2:c.15333+123del XP_016856319.2:n.15333+123del
NM_020765.3:c.15324+123del MANE Select NP_065816.2:n.15324+123del