Canonical Allele Identifier: CA2643751623
Gene: UBR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19078358_19078380del , CM000663.2:g.19078358_19078380del GRCh38
NC_000001.10:g.19404852_19404874del , CM000663.1:g.19404852_19404874del GRCh37
NC_000001.9:g.19277439_19277461del NCBI36
NG_027669.1:g.136876_136898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15234-311_15234-289del MANE Select ENSP00000364403.3:n.15234-311_15234-289del
ENST00000375224.1:c.2355-311_2355-289del ENSP00000364372.1:n.2355-311_2355-289del
ENST00000375225.7:c.459-311_459-289del ENSP00000364373.3:n.459-311_459-289del
ENST00000375254.7:c.15234-311_15234-289del ENSP00000364403.3:n.15234-311_15234-289del
ENST00000459947.5:n.2930_2952del
NM_020765.2:c.15234-311_15234-289del NP_065816.2:n.15234-311_15234-289del
XM_011541108.1:c.15387-311_15387-289del XP_011539410.1:n.15387-311_15387-289del
XM_011541109.1:c.15384-311_15384-289del XP_011539411.1:n.15384-311_15384-289del
XM_011541110.1:c.15384-311_15384-289del XP_011539412.1:n.15384-311_15384-289del
XM_011541111.1:c.15384-311_15384-289del XP_011539413.1:n.15384-311_15384-289del
XM_011541112.1:c.15372-311_15372-289del XP_011539414.1:n.15372-311_15372-289del
XM_011541113.1:c.15369-311_15369-289del XP_011539415.1:n.15369-311_15369-289del
XM_011541114.1:c.15369-311_15369-289del XP_011539416.1:n.15369-311_15369-289del
XM_011541115.1:c.15363-311_15363-289del XP_011539417.1:n.15363-311_15363-289del
XM_011541116.1:c.15354-311_15354-289del XP_011539418.1:n.15354-311_15354-289del
XM_011541117.1:c.15303-311_15303-289del XP_011539419.1:n.15303-311_15303-289del
XM_011541118.1:c.15300-311_15300-289del XP_011539420.1:n.15300-311_15300-289del
XM_011541119.1:c.15267-311_15267-289del XP_011539421.1:n.15267-311_15267-289del
XM_011541120.1:c.15264-311_15264-289del XP_011539422.1:n.15264-311_15264-289del
XM_011541121.1:c.15231-311_15231-289del XP_011539423.1:n.15231-311_15231-289del
XM_011541108.3:c.15501-311_15501-289del XP_011539410.2:n.15501-311_15501-289del
XM_011541109.3:c.15498-311_15498-289del XP_011539411.2:n.15498-311_15498-289del
XM_011541110.3:c.15498-311_15498-289del XP_011539412.2:n.15498-311_15498-289del
XM_011541111.3:c.15498-311_15498-289del XP_011539413.2:n.15498-311_15498-289del
XM_011541112.3:c.15486-311_15486-289del XP_011539414.2:n.15486-311_15486-289del
XM_011541113.3:c.15483-311_15483-289del XP_011539415.2:n.15483-311_15483-289del
XM_011541114.3:c.15483-311_15483-289del XP_011539416.2:n.15483-311_15483-289del
XM_011541115.3:c.15477-311_15477-289del XP_011539417.2:n.15477-311_15477-289del
XM_011541116.3:c.15468-311_15468-289del XP_011539418.2:n.15468-311_15468-289del
XM_011541117.3:c.15417-311_15417-289del XP_011539419.2:n.15417-311_15417-289del
XM_011541118.3:c.15414-311_15414-289del XP_011539420.2:n.15414-311_15414-289del
XM_011541119.3:c.15381-311_15381-289del XP_011539421.2:n.15381-311_15381-289del
XM_011541120.3:c.15378-311_15378-289del XP_011539422.2:n.15378-311_15378-289del
XM_011541121.3:c.15345-311_15345-289del XP_011539423.2:n.15345-311_15345-289del
XM_017000822.2:c.15480-311_15480-289del XP_016856311.2:n.15480-311_15480-289del
XM_017000823.2:c.15453-311_15453-289del XP_016856312.2:n.15453-311_15453-289del
XM_017000824.2:c.15399-311_15399-289del XP_016856313.2:n.15399-311_15399-289del
XM_017000825.2:c.15384-311_15384-289del XP_016856314.2:n.15384-311_15384-289del
XM_017000826.2:c.15381-311_15381-289del XP_016856315.2:n.15381-311_15381-289del
XM_017000827.2:c.15366-311_15366-289del XP_016856316.2:n.15366-311_15366-289del
XM_017000828.2:c.15342-311_15342-289del XP_016856317.2:n.15342-311_15342-289del
XM_017000829.2:c.15294-311_15294-289del XP_016856318.2:n.15294-311_15294-289del
XM_017000830.2:c.15243-311_15243-289del XP_016856319.2:n.15243-311_15243-289del
NM_020765.3:c.15234-311_15234-289del MANE Select NP_065816.2:n.15234-311_15234-289del