Canonical Allele Identifier: CA2643751618
Gene: UBR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19078348_19078359del , CM000663.2:g.19078348_19078359del GRCh38
NC_000001.10:g.19404842_19404853del , CM000663.1:g.19404842_19404853del GRCh37
NC_000001.9:g.19277429_19277440del NCBI36
NG_027669.1:g.136894_136905del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15234-293_15234-282del MANE Select ENSP00000364403.3:n.15234-293_15234-282del
ENST00000375224.1:c.2355-293_2355-282del ENSP00000364372.1:n.2355-293_2355-282del
ENST00000375225.7:c.459-293_459-282del ENSP00000364373.3:n.459-293_459-282del
ENST00000375254.7:c.15234-293_15234-282del ENSP00000364403.3:n.15234-293_15234-282del
ENST00000459947.5:n.2948_2959del
NM_020765.2:c.15234-293_15234-282del NP_065816.2:n.15234-293_15234-282del
XM_011541108.1:c.15387-293_15387-282del XP_011539410.1:n.15387-293_15387-282del
XM_011541109.1:c.15384-293_15384-282del XP_011539411.1:n.15384-293_15384-282del
XM_011541110.1:c.15384-293_15384-282del XP_011539412.1:n.15384-293_15384-282del
XM_011541111.1:c.15384-293_15384-282del XP_011539413.1:n.15384-293_15384-282del
XM_011541112.1:c.15372-293_15372-282del XP_011539414.1:n.15372-293_15372-282del
XM_011541113.1:c.15369-293_15369-282del XP_011539415.1:n.15369-293_15369-282del
XM_011541114.1:c.15369-293_15369-282del XP_011539416.1:n.15369-293_15369-282del
XM_011541115.1:c.15363-293_15363-282del XP_011539417.1:n.15363-293_15363-282del
XM_011541116.1:c.15354-293_15354-282del XP_011539418.1:n.15354-293_15354-282del
XM_011541117.1:c.15303-293_15303-282del XP_011539419.1:n.15303-293_15303-282del
XM_011541118.1:c.15300-293_15300-282del XP_011539420.1:n.15300-293_15300-282del
XM_011541119.1:c.15267-293_15267-282del XP_011539421.1:n.15267-293_15267-282del
XM_011541120.1:c.15264-293_15264-282del XP_011539422.1:n.15264-293_15264-282del
XM_011541121.1:c.15231-293_15231-282del XP_011539423.1:n.15231-293_15231-282del
XM_011541108.3:c.15501-293_15501-282del XP_011539410.2:n.15501-293_15501-282del
XM_011541109.3:c.15498-293_15498-282del XP_011539411.2:n.15498-293_15498-282del
XM_011541110.3:c.15498-293_15498-282del XP_011539412.2:n.15498-293_15498-282del
XM_011541111.3:c.15498-293_15498-282del XP_011539413.2:n.15498-293_15498-282del
XM_011541112.3:c.15486-293_15486-282del XP_011539414.2:n.15486-293_15486-282del
XM_011541113.3:c.15483-293_15483-282del XP_011539415.2:n.15483-293_15483-282del
XM_011541114.3:c.15483-293_15483-282del XP_011539416.2:n.15483-293_15483-282del
XM_011541115.3:c.15477-293_15477-282del XP_011539417.2:n.15477-293_15477-282del
XM_011541116.3:c.15468-293_15468-282del XP_011539418.2:n.15468-293_15468-282del
XM_011541117.3:c.15417-293_15417-282del XP_011539419.2:n.15417-293_15417-282del
XM_011541118.3:c.15414-293_15414-282del XP_011539420.2:n.15414-293_15414-282del
XM_011541119.3:c.15381-293_15381-282del XP_011539421.2:n.15381-293_15381-282del
XM_011541120.3:c.15378-293_15378-282del XP_011539422.2:n.15378-293_15378-282del
XM_011541121.3:c.15345-293_15345-282del XP_011539423.2:n.15345-293_15345-282del
XM_017000822.2:c.15480-293_15480-282del XP_016856311.2:n.15480-293_15480-282del
XM_017000823.2:c.15453-293_15453-282del XP_016856312.2:n.15453-293_15453-282del
XM_017000824.2:c.15399-293_15399-282del XP_016856313.2:n.15399-293_15399-282del
XM_017000825.2:c.15384-293_15384-282del XP_016856314.2:n.15384-293_15384-282del
XM_017000826.2:c.15381-293_15381-282del XP_016856315.2:n.15381-293_15381-282del
XM_017000827.2:c.15366-293_15366-282del XP_016856316.2:n.15366-293_15366-282del
XM_017000828.2:c.15342-293_15342-282del XP_016856317.2:n.15342-293_15342-282del
XM_017000829.2:c.15294-293_15294-282del XP_016856318.2:n.15294-293_15294-282del
XM_017000830.2:c.15243-293_15243-282del XP_016856319.2:n.15243-293_15243-282del
NM_020765.3:c.15234-293_15234-282del MANE Select NP_065816.2:n.15234-293_15234-282del