Canonical Allele Identifier: CA18791207

Gene: UBR4

Linked Data

• dbSNP Id: rs958101185
• MyVariant Identifiers: chr1:g.19404743_19404745del (hg19) ; chr1:g.19078249_19078251del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078251_19078253del , CM000663.2:g.19078251_19078253del	GRCh38
NC_000001.10:g.19404745_19404747del , CM000663.1:g.19404745_19404747del	GRCh37
NC_000001.9:g.19277332_19277334del	NCBI36
NG_027669.1:g.137002_137004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234-185_15234-183del MANE Select	ENSP00000364403.3:n.15234-185_15234-183del
ENST00000375224.1:c.2355-185_2355-183del	ENSP00000364372.1:n.2355-185_2355-183del
ENST00000375225.7:c.459-185_459-183del	ENSP00000364373.3:n.459-185_459-183del
ENST00000375254.7:c.15234-185_15234-183del	ENSP00000364403.3:n.15234-185_15234-183del
ENST00000459947.5:n.3056_3058del
NM_020765.2:c.15234-185_15234-183del	NP_065816.2:n.15234-185_15234-183del
XM_011541108.1:c.15387-185_15387-183del	XP_011539410.1:n.15387-185_15387-183del
XM_011541109.1:c.15384-185_15384-183del	XP_011539411.1:n.15384-185_15384-183del
XM_011541110.1:c.15384-185_15384-183del	XP_011539412.1:n.15384-185_15384-183del
XM_011541111.1:c.15384-185_15384-183del	XP_011539413.1:n.15384-185_15384-183del
XM_011541112.1:c.15372-185_15372-183del	XP_011539414.1:n.15372-185_15372-183del
XM_011541113.1:c.15369-185_15369-183del	XP_011539415.1:n.15369-185_15369-183del
XM_011541114.1:c.15369-185_15369-183del	XP_011539416.1:n.15369-185_15369-183del
XM_011541115.1:c.15363-185_15363-183del	XP_011539417.1:n.15363-185_15363-183del
XM_011541116.1:c.15354-185_15354-183del	XP_011539418.1:n.15354-185_15354-183del
XM_011541117.1:c.15303-185_15303-183del	XP_011539419.1:n.15303-185_15303-183del
XM_011541118.1:c.15300-185_15300-183del	XP_011539420.1:n.15300-185_15300-183del
XM_011541119.1:c.15267-185_15267-183del	XP_011539421.1:n.15267-185_15267-183del
XM_011541120.1:c.15264-185_15264-183del	XP_011539422.1:n.15264-185_15264-183del
XM_011541121.1:c.15231-185_15231-183del	XP_011539423.1:n.15231-185_15231-183del
XM_011541108.3:c.15501-185_15501-183del	XP_011539410.2:n.15501-185_15501-183del
XM_011541109.3:c.15498-185_15498-183del	XP_011539411.2:n.15498-185_15498-183del
XM_011541110.3:c.15498-185_15498-183del	XP_011539412.2:n.15498-185_15498-183del
XM_011541111.3:c.15498-185_15498-183del	XP_011539413.2:n.15498-185_15498-183del
XM_011541112.3:c.15486-185_15486-183del	XP_011539414.2:n.15486-185_15486-183del
XM_011541113.3:c.15483-185_15483-183del	XP_011539415.2:n.15483-185_15483-183del
XM_011541114.3:c.15483-185_15483-183del	XP_011539416.2:n.15483-185_15483-183del
XM_011541115.3:c.15477-185_15477-183del	XP_011539417.2:n.15477-185_15477-183del
XM_011541116.3:c.15468-185_15468-183del	XP_011539418.2:n.15468-185_15468-183del
XM_011541117.3:c.15417-185_15417-183del	XP_011539419.2:n.15417-185_15417-183del
XM_011541118.3:c.15414-185_15414-183del	XP_011539420.2:n.15414-185_15414-183del
XM_011541119.3:c.15381-185_15381-183del	XP_011539421.2:n.15381-185_15381-183del
XM_011541120.3:c.15378-185_15378-183del	XP_011539422.2:n.15378-185_15378-183del
XM_011541121.3:c.15345-185_15345-183del	XP_011539423.2:n.15345-185_15345-183del
XM_017000822.2:c.15480-185_15480-183del	XP_016856311.2:n.15480-185_15480-183del
XM_017000823.2:c.15453-185_15453-183del	XP_016856312.2:n.15453-185_15453-183del
XM_017000824.2:c.15399-185_15399-183del	XP_016856313.2:n.15399-185_15399-183del
XM_017000825.2:c.15384-185_15384-183del	XP_016856314.2:n.15384-185_15384-183del
XM_017000826.2:c.15381-185_15381-183del	XP_016856315.2:n.15381-185_15381-183del
XM_017000827.2:c.15366-185_15366-183del	XP_016856316.2:n.15366-185_15366-183del
XM_017000828.2:c.15342-185_15342-183del	XP_016856317.2:n.15342-185_15342-183del
XM_017000829.2:c.15294-185_15294-183del	XP_016856318.2:n.15294-185_15294-183del
XM_017000830.2:c.15243-185_15243-183del	XP_016856319.2:n.15243-185_15243-183del
NM_020765.3:c.15234-185_15234-183del MANE Select	NP_065816.2:n.15234-185_15234-183del