Canonical Allele Identifier: CA1156956228

Gene: UBR4

Linked Data

• dbSNP Id: rs2076169850

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078412_19078422del , CM000663.2:g.19078412_19078422del	GRCh38
NC_000001.10:g.19404906_19404916del , CM000663.1:g.19404906_19404916del	GRCh37
NC_000001.9:g.19277493_19277503del	NCBI36
NG_027669.1:g.136831_136841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234-356_15234-346del MANE Select	ENSP00000364403.3:n.15234-356_15234-346del
ENST00000375224.1:c.2355-356_2355-346del	ENSP00000364372.1:n.2355-356_2355-346del
ENST00000375225.7:c.459-356_459-346del	ENSP00000364373.3:n.459-356_459-346del
ENST00000375254.7:c.15234-356_15234-346del	ENSP00000364403.3:n.15234-356_15234-346del
ENST00000459947.5:n.2885_2895del
NM_020765.2:c.15234-356_15234-346del	NP_065816.2:n.15234-356_15234-346del
XM_011541108.1:c.15387-356_15387-346del	XP_011539410.1:n.15387-356_15387-346del
XM_011541109.1:c.15384-356_15384-346del	XP_011539411.1:n.15384-356_15384-346del
XM_011541110.1:c.15384-356_15384-346del	XP_011539412.1:n.15384-356_15384-346del
XM_011541111.1:c.15384-356_15384-346del	XP_011539413.1:n.15384-356_15384-346del
XM_011541112.1:c.15372-356_15372-346del	XP_011539414.1:n.15372-356_15372-346del
XM_011541113.1:c.15369-356_15369-346del	XP_011539415.1:n.15369-356_15369-346del
XM_011541114.1:c.15369-356_15369-346del	XP_011539416.1:n.15369-356_15369-346del
XM_011541115.1:c.15363-356_15363-346del	XP_011539417.1:n.15363-356_15363-346del
XM_011541116.1:c.15354-356_15354-346del	XP_011539418.1:n.15354-356_15354-346del
XM_011541117.1:c.15303-356_15303-346del	XP_011539419.1:n.15303-356_15303-346del
XM_011541118.1:c.15300-356_15300-346del	XP_011539420.1:n.15300-356_15300-346del
XM_011541119.1:c.15267-356_15267-346del	XP_011539421.1:n.15267-356_15267-346del
XM_011541120.1:c.15264-356_15264-346del	XP_011539422.1:n.15264-356_15264-346del
XM_011541121.1:c.15231-356_15231-346del	XP_011539423.1:n.15231-356_15231-346del
XM_011541108.3:c.15501-356_15501-346del	XP_011539410.2:n.15501-356_15501-346del
XM_011541109.3:c.15498-356_15498-346del	XP_011539411.2:n.15498-356_15498-346del
XM_011541110.3:c.15498-356_15498-346del	XP_011539412.2:n.15498-356_15498-346del
XM_011541111.3:c.15498-356_15498-346del	XP_011539413.2:n.15498-356_15498-346del
XM_011541112.3:c.15486-356_15486-346del	XP_011539414.2:n.15486-356_15486-346del
XM_011541113.3:c.15483-356_15483-346del	XP_011539415.2:n.15483-356_15483-346del
XM_011541114.3:c.15483-356_15483-346del	XP_011539416.2:n.15483-356_15483-346del
XM_011541115.3:c.15477-356_15477-346del	XP_011539417.2:n.15477-356_15477-346del
XM_011541116.3:c.15468-356_15468-346del	XP_011539418.2:n.15468-356_15468-346del
XM_011541117.3:c.15417-356_15417-346del	XP_011539419.2:n.15417-356_15417-346del
XM_011541118.3:c.15414-356_15414-346del	XP_011539420.2:n.15414-356_15414-346del
XM_011541119.3:c.15381-356_15381-346del	XP_011539421.2:n.15381-356_15381-346del
XM_011541120.3:c.15378-356_15378-346del	XP_011539422.2:n.15378-356_15378-346del
XM_011541121.3:c.15345-356_15345-346del	XP_011539423.2:n.15345-356_15345-346del
XM_017000822.2:c.15480-356_15480-346del	XP_016856311.2:n.15480-356_15480-346del
XM_017000823.2:c.15453-356_15453-346del	XP_016856312.2:n.15453-356_15453-346del
XM_017000824.2:c.15399-356_15399-346del	XP_016856313.2:n.15399-356_15399-346del
XM_017000825.2:c.15384-356_15384-346del	XP_016856314.2:n.15384-356_15384-346del
XM_017000826.2:c.15381-356_15381-346del	XP_016856315.2:n.15381-356_15381-346del
XM_017000827.2:c.15366-356_15366-346del	XP_016856316.2:n.15366-356_15366-346del
XM_017000828.2:c.15342-356_15342-346del	XP_016856317.2:n.15342-356_15342-346del
XM_017000829.2:c.15294-356_15294-346del	XP_016856318.2:n.15294-356_15294-346del
XM_017000830.2:c.15243-356_15243-346del	XP_016856319.2:n.15243-356_15243-346del
NM_020765.3:c.15234-356_15234-346del MANE Select	NP_065816.2:n.15234-356_15234-346del