Canonical Allele Identifier: CA1156956125

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078147_19078148delinsAG , CM000663.2:g.19078147_19078148delinsAG	GRCh38
NC_000001.10:g.19404641_19404642delinsAG , CM000663.1:g.19404641_19404642delinsAG	GRCh37
NC_000001.9:g.19277228_19277229delinsAG	NCBI36
NG_027669.1:g.137105_137106delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234-82_15234-81delinsCT MANE Select	ENSP00000364403.3:n.15234-82_15234-81delinsCT
ENST00000375224.1:c.2355-82_2355-81delinsCT	ENSP00000364372.1:n.2355-82_2355-81delinsCT
ENST00000375225.7:c.459-82_459-81delinsCT	ENSP00000364373.3:n.459-82_459-81delinsCT
ENST00000375254.7:c.15234-82_15234-81delinsCT	ENSP00000364403.3:n.15234-82_15234-81delinsCT
ENST00000459947.5:n.3159_3160delinsCT
NM_020765.2:c.15234-82_15234-81delinsCT	NP_065816.2:n.15234-82_15234-81delinsCT
XM_011541108.1:c.15387-82_15387-81delinsCT	XP_011539410.1:n.15387-82_15387-81delinsCT
XM_011541109.1:c.15384-82_15384-81delinsCT	XP_011539411.1:n.15384-82_15384-81delinsCT
XM_011541110.1:c.15384-82_15384-81delinsCT	XP_011539412.1:n.15384-82_15384-81delinsCT
XM_011541111.1:c.15384-82_15384-81delinsCT	XP_011539413.1:n.15384-82_15384-81delinsCT
XM_011541112.1:c.15372-82_15372-81delinsCT	XP_011539414.1:n.15372-82_15372-81delinsCT
XM_011541113.1:c.15369-82_15369-81delinsCT	XP_011539415.1:n.15369-82_15369-81delinsCT
XM_011541114.1:c.15369-82_15369-81delinsCT	XP_011539416.1:n.15369-82_15369-81delinsCT
XM_011541115.1:c.15363-82_15363-81delinsCT	XP_011539417.1:n.15363-82_15363-81delinsCT
XM_011541116.1:c.15354-82_15354-81delinsCT	XP_011539418.1:n.15354-82_15354-81delinsCT
XM_011541117.1:c.15303-82_15303-81delinsCT	XP_011539419.1:n.15303-82_15303-81delinsCT
XM_011541118.1:c.15300-82_15300-81delinsCT	XP_011539420.1:n.15300-82_15300-81delinsCT
XM_011541119.1:c.15267-82_15267-81delinsCT	XP_011539421.1:n.15267-82_15267-81delinsCT
XM_011541120.1:c.15264-82_15264-81delinsCT	XP_011539422.1:n.15264-82_15264-81delinsCT
XM_011541121.1:c.15231-82_15231-81delinsCT	XP_011539423.1:n.15231-82_15231-81delinsCT
XM_011541108.3:c.15501-82_15501-81delinsCT	XP_011539410.2:n.15501-82_15501-81delinsCT
XM_011541109.3:c.15498-82_15498-81delinsCT	XP_011539411.2:n.15498-82_15498-81delinsCT
XM_011541110.3:c.15498-82_15498-81delinsCT	XP_011539412.2:n.15498-82_15498-81delinsCT
XM_011541111.3:c.15498-82_15498-81delinsCT	XP_011539413.2:n.15498-82_15498-81delinsCT
XM_011541112.3:c.15486-82_15486-81delinsCT	XP_011539414.2:n.15486-82_15486-81delinsCT
XM_011541113.3:c.15483-82_15483-81delinsCT	XP_011539415.2:n.15483-82_15483-81delinsCT
XM_011541114.3:c.15483-82_15483-81delinsCT	XP_011539416.2:n.15483-82_15483-81delinsCT
XM_011541115.3:c.15477-82_15477-81delinsCT	XP_011539417.2:n.15477-82_15477-81delinsCT
XM_011541116.3:c.15468-82_15468-81delinsCT	XP_011539418.2:n.15468-82_15468-81delinsCT
XM_011541117.3:c.15417-82_15417-81delinsCT	XP_011539419.2:n.15417-82_15417-81delinsCT
XM_011541118.3:c.15414-82_15414-81delinsCT	XP_011539420.2:n.15414-82_15414-81delinsCT
XM_011541119.3:c.15381-82_15381-81delinsCT	XP_011539421.2:n.15381-82_15381-81delinsCT
XM_011541120.3:c.15378-82_15378-81delinsCT	XP_011539422.2:n.15378-82_15378-81delinsCT
XM_011541121.3:c.15345-82_15345-81delinsCT	XP_011539423.2:n.15345-82_15345-81delinsCT
XM_017000822.2:c.15480-82_15480-81delinsCT	XP_016856311.2:n.15480-82_15480-81delinsCT
XM_017000823.2:c.15453-82_15453-81delinsCT	XP_016856312.2:n.15453-82_15453-81delinsCT
XM_017000824.2:c.15399-82_15399-81delinsCT	XP_016856313.2:n.15399-82_15399-81delinsCT
XM_017000825.2:c.15384-82_15384-81delinsCT	XP_016856314.2:n.15384-82_15384-81delinsCT
XM_017000826.2:c.15381-82_15381-81delinsCT	XP_016856315.2:n.15381-82_15381-81delinsCT
XM_017000827.2:c.15366-82_15366-81delinsCT	XP_016856316.2:n.15366-82_15366-81delinsCT
XM_017000828.2:c.15342-82_15342-81delinsCT	XP_016856317.2:n.15342-82_15342-81delinsCT
XM_017000829.2:c.15294-82_15294-81delinsCT	XP_016856318.2:n.15294-82_15294-81delinsCT
XM_017000830.2:c.15243-82_15243-81delinsCT	XP_016856319.2:n.15243-82_15243-81delinsCT
NM_020765.3:c.15234-82_15234-81delinsCT MANE Select	NP_065816.2:n.15234-82_15234-81delinsCT