Canonical Allele Identifier: CA2742695869

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078195_19078205del , CM000663.2:g.19078195_19078205del	GRCh38
NC_000001.10:g.19404689_19404699del , CM000663.1:g.19404689_19404699del	GRCh37
NC_000001.9:g.19277276_19277286del	NCBI36
NG_027669.1:g.137048_137058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234-139_15234-129del MANE Select	ENSP00000364403.3:n.15234-139_15234-129del
ENST00000375224.1:c.2355-139_2355-129del	ENSP00000364372.1:n.2355-139_2355-129del
ENST00000375225.7:c.459-139_459-129del	ENSP00000364373.3:n.459-139_459-129del
ENST00000375254.7:c.15234-139_15234-129del	ENSP00000364403.3:n.15234-139_15234-129del
ENST00000459947.5:n.3102_3112del
NM_020765.2:c.15234-139_15234-129del	NP_065816.2:n.15234-139_15234-129del
XM_011541108.1:c.15387-139_15387-129del	XP_011539410.1:n.15387-139_15387-129del
XM_011541109.1:c.15384-139_15384-129del	XP_011539411.1:n.15384-139_15384-129del
XM_011541110.1:c.15384-139_15384-129del	XP_011539412.1:n.15384-139_15384-129del
XM_011541111.1:c.15384-139_15384-129del	XP_011539413.1:n.15384-139_15384-129del
XM_011541112.1:c.15372-139_15372-129del	XP_011539414.1:n.15372-139_15372-129del
XM_011541113.1:c.15369-139_15369-129del	XP_011539415.1:n.15369-139_15369-129del
XM_011541114.1:c.15369-139_15369-129del	XP_011539416.1:n.15369-139_15369-129del
XM_011541115.1:c.15363-139_15363-129del	XP_011539417.1:n.15363-139_15363-129del
XM_011541116.1:c.15354-139_15354-129del	XP_011539418.1:n.15354-139_15354-129del
XM_011541117.1:c.15303-139_15303-129del	XP_011539419.1:n.15303-139_15303-129del
XM_011541118.1:c.15300-139_15300-129del	XP_011539420.1:n.15300-139_15300-129del
XM_011541119.1:c.15267-139_15267-129del	XP_011539421.1:n.15267-139_15267-129del
XM_011541120.1:c.15264-139_15264-129del	XP_011539422.1:n.15264-139_15264-129del
XM_011541121.1:c.15231-139_15231-129del	XP_011539423.1:n.15231-139_15231-129del
XM_011541108.3:c.15501-139_15501-129del	XP_011539410.2:n.15501-139_15501-129del
XM_011541109.3:c.15498-139_15498-129del	XP_011539411.2:n.15498-139_15498-129del
XM_011541110.3:c.15498-139_15498-129del	XP_011539412.2:n.15498-139_15498-129del
XM_011541111.3:c.15498-139_15498-129del	XP_011539413.2:n.15498-139_15498-129del
XM_011541112.3:c.15486-139_15486-129del	XP_011539414.2:n.15486-139_15486-129del
XM_011541113.3:c.15483-139_15483-129del	XP_011539415.2:n.15483-139_15483-129del
XM_011541114.3:c.15483-139_15483-129del	XP_011539416.2:n.15483-139_15483-129del
XM_011541115.3:c.15477-139_15477-129del	XP_011539417.2:n.15477-139_15477-129del
XM_011541116.3:c.15468-139_15468-129del	XP_011539418.2:n.15468-139_15468-129del
XM_011541117.3:c.15417-139_15417-129del	XP_011539419.2:n.15417-139_15417-129del
XM_011541118.3:c.15414-139_15414-129del	XP_011539420.2:n.15414-139_15414-129del
XM_011541119.3:c.15381-139_15381-129del	XP_011539421.2:n.15381-139_15381-129del
XM_011541120.3:c.15378-139_15378-129del	XP_011539422.2:n.15378-139_15378-129del
XM_011541121.3:c.15345-139_15345-129del	XP_011539423.2:n.15345-139_15345-129del
XM_017000822.2:c.15480-139_15480-129del	XP_016856311.2:n.15480-139_15480-129del
XM_017000823.2:c.15453-139_15453-129del	XP_016856312.2:n.15453-139_15453-129del
XM_017000824.2:c.15399-139_15399-129del	XP_016856313.2:n.15399-139_15399-129del
XM_017000825.2:c.15384-139_15384-129del	XP_016856314.2:n.15384-139_15384-129del
XM_017000826.2:c.15381-139_15381-129del	XP_016856315.2:n.15381-139_15381-129del
XM_017000827.2:c.15366-139_15366-129del	XP_016856316.2:n.15366-139_15366-129del
XM_017000828.2:c.15342-139_15342-129del	XP_016856317.2:n.15342-139_15342-129del
XM_017000829.2:c.15294-139_15294-129del	XP_016856318.2:n.15294-139_15294-129del
XM_017000830.2:c.15243-139_15243-129del	XP_016856319.2:n.15243-139_15243-129del
NM_020765.3:c.15234-139_15234-129del MANE Select	NP_065816.2:n.15234-139_15234-129del