Canonical Allele Identifier: CA521500168
Gene: UBR4 HGNC NCBI

Linked Data

dbSNP Id: rs1450016531

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19078368_19078386del , CM000663.2:g.19078368_19078386del GRCh38
NC_000001.10:g.19404862_19404880del , CM000663.1:g.19404862_19404880del GRCh37
NC_000001.9:g.19277449_19277467del NCBI36
NG_027669.1:g.136868_136886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15234-319_15234-301del MANE Select ENSP00000364403.3:n.15234-319_15234-301del
ENST00000375224.1:c.2355-319_2355-301del ENSP00000364372.1:n.2355-319_2355-301del
ENST00000375225.7:c.459-319_459-301del ENSP00000364373.3:n.459-319_459-301del
ENST00000375254.7:c.15234-319_15234-301del ENSP00000364403.3:n.15234-319_15234-301del
ENST00000459947.5:n.2922_2940del
NM_020765.2:c.15234-319_15234-301del NP_065816.2:n.15234-319_15234-301del
XM_011541108.1:c.15387-319_15387-301del XP_011539410.1:n.15387-319_15387-301del
XM_011541109.1:c.15384-319_15384-301del XP_011539411.1:n.15384-319_15384-301del
XM_011541110.1:c.15384-319_15384-301del XP_011539412.1:n.15384-319_15384-301del
XM_011541111.1:c.15384-319_15384-301del XP_011539413.1:n.15384-319_15384-301del
XM_011541112.1:c.15372-319_15372-301del XP_011539414.1:n.15372-319_15372-301del
XM_011541113.1:c.15369-319_15369-301del XP_011539415.1:n.15369-319_15369-301del
XM_011541114.1:c.15369-319_15369-301del XP_011539416.1:n.15369-319_15369-301del
XM_011541115.1:c.15363-319_15363-301del XP_011539417.1:n.15363-319_15363-301del
XM_011541116.1:c.15354-319_15354-301del XP_011539418.1:n.15354-319_15354-301del
XM_011541117.1:c.15303-319_15303-301del XP_011539419.1:n.15303-319_15303-301del
XM_011541118.1:c.15300-319_15300-301del XP_011539420.1:n.15300-319_15300-301del
XM_011541119.1:c.15267-319_15267-301del XP_011539421.1:n.15267-319_15267-301del
XM_011541120.1:c.15264-319_15264-301del XP_011539422.1:n.15264-319_15264-301del
XM_011541121.1:c.15231-319_15231-301del XP_011539423.1:n.15231-319_15231-301del
XM_011541108.3:c.15501-319_15501-301del XP_011539410.2:n.15501-319_15501-301del
XM_011541109.3:c.15498-319_15498-301del XP_011539411.2:n.15498-319_15498-301del
XM_011541110.3:c.15498-319_15498-301del XP_011539412.2:n.15498-319_15498-301del
XM_011541111.3:c.15498-319_15498-301del XP_011539413.2:n.15498-319_15498-301del
XM_011541112.3:c.15486-319_15486-301del XP_011539414.2:n.15486-319_15486-301del
XM_011541113.3:c.15483-319_15483-301del XP_011539415.2:n.15483-319_15483-301del
XM_011541114.3:c.15483-319_15483-301del XP_011539416.2:n.15483-319_15483-301del
XM_011541115.3:c.15477-319_15477-301del XP_011539417.2:n.15477-319_15477-301del
XM_011541116.3:c.15468-319_15468-301del XP_011539418.2:n.15468-319_15468-301del
XM_011541117.3:c.15417-319_15417-301del XP_011539419.2:n.15417-319_15417-301del
XM_011541118.3:c.15414-319_15414-301del XP_011539420.2:n.15414-319_15414-301del
XM_011541119.3:c.15381-319_15381-301del XP_011539421.2:n.15381-319_15381-301del
XM_011541120.3:c.15378-319_15378-301del XP_011539422.2:n.15378-319_15378-301del
XM_011541121.3:c.15345-319_15345-301del XP_011539423.2:n.15345-319_15345-301del
XM_017000822.2:c.15480-319_15480-301del XP_016856311.2:n.15480-319_15480-301del
XM_017000823.2:c.15453-319_15453-301del XP_016856312.2:n.15453-319_15453-301del
XM_017000824.2:c.15399-319_15399-301del XP_016856313.2:n.15399-319_15399-301del
XM_017000825.2:c.15384-319_15384-301del XP_016856314.2:n.15384-319_15384-301del
XM_017000826.2:c.15381-319_15381-301del XP_016856315.2:n.15381-319_15381-301del
XM_017000827.2:c.15366-319_15366-301del XP_016856316.2:n.15366-319_15366-301del
XM_017000828.2:c.15342-319_15342-301del XP_016856317.2:n.15342-319_15342-301del
XM_017000829.2:c.15294-319_15294-301del XP_016856318.2:n.15294-319_15294-301del
XM_017000830.2:c.15243-319_15243-301del XP_016856319.2:n.15243-319_15243-301del
NM_020765.3:c.15234-319_15234-301del MANE Select NP_065816.2:n.15234-319_15234-301del