Canonical Allele Identifier: CA1144402372

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078040T= , CM000663.2:g.19078040T=	GRCh38
NC_000001.10:g.19404534T= , CM000663.1:g.19404534T=	GRCh37
NC_000001.9:g.19277121T=	NCBI36
NG_027669.1:g.137213A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15260A= MANE Select	ENSP00000364403.3:p.Tyr5087=
ENST00000375224.1:c.2381A=	ENSP00000364372.1:p.Tyr794=
ENST00000375225.7:c.485A=	ENSP00000364373.3:p.Tyr162=
ENST00000375254.7:c.15260A=	ENSP00000364403.3:p.Tyr5087=
ENST00000459947.5:n.3267A=
NM_020765.2:c.15260A=	NP_065816.2:p.Tyr5087=
XM_011541108.1:c.15413A=	XP_011539410.1:p.Tyr5138=
XM_011541109.1:c.15410A=	XP_011539411.1:p.Tyr5137=
XM_011541110.1:c.15410A=	XP_011539412.1:p.Tyr5137=
XM_011541111.1:c.15410A=	XP_011539413.1:p.Tyr5137=
XM_011541112.1:c.15398A=	XP_011539414.1:p.Tyr5133=
XM_011541113.1:c.15395A=	XP_011539415.1:p.Tyr5132=
XM_011541114.1:c.15395A=	XP_011539416.1:p.Tyr5132=
XM_011541115.1:c.15389A=	XP_011539417.1:p.Tyr5130=
XM_011541116.1:c.15380A=	XP_011539418.1:p.Tyr5127=
XM_011541117.1:c.15329A=	XP_011539419.1:p.Tyr5110=
XM_011541118.1:c.15326A=	XP_011539420.1:p.Tyr5109=
XM_011541119.1:c.15293A=	XP_011539421.1:p.Tyr5098=
XM_011541120.1:c.15290A=	XP_011539422.1:p.Tyr5097=
XM_011541121.1:c.15257A=	XP_011539423.1:p.Tyr5086=
XM_011541108.3:c.15527A=	XP_011539410.2:p.Tyr5176=
XM_011541109.3:c.15524A=	XP_011539411.2:p.Tyr5175=
XM_011541110.3:c.15524A=	XP_011539412.2:p.Tyr5175=
XM_011541111.3:c.15524A=	XP_011539413.2:p.Tyr5175=
XM_011541112.3:c.15512A=	XP_011539414.2:p.Tyr5171=
XM_011541113.3:c.15509A=	XP_011539415.2:p.Tyr5170=
XM_011541114.3:c.15509A=	XP_011539416.2:p.Tyr5170=
XM_011541115.3:c.15503A=	XP_011539417.2:p.Tyr5168=
XM_011541116.3:c.15494A=	XP_011539418.2:p.Tyr5165=
XM_011541117.3:c.15443A=	XP_011539419.2:p.Tyr5148=
XM_011541118.3:c.15440A=	XP_011539420.2:p.Tyr5147=
XM_011541119.3:c.15407A=	XP_011539421.2:p.Tyr5136=
XM_011541120.3:c.15404A=	XP_011539422.2:p.Tyr5135=
XM_011541121.3:c.15371A=	XP_011539423.2:p.Tyr5124=
XM_017000822.2:c.15506A=	XP_016856311.2:p.Tyr5169=
XM_017000823.2:c.15479A=	XP_016856312.2:p.Tyr5160=
XM_017000824.2:c.15425A=	XP_016856313.2:p.Tyr5142=
XM_017000825.2:c.15410A=	XP_016856314.2:p.Tyr5137=
XM_017000826.2:c.15407A=	XP_016856315.2:p.Tyr5136=
XM_017000827.2:c.15392A=	XP_016856316.2:p.Tyr5131=
XM_017000828.2:c.15368A=	XP_016856317.2:p.Tyr5123=
XM_017000829.2:c.15320A=	XP_016856318.2:p.Tyr5107=
XM_017000830.2:c.15269A=	XP_016856319.2:p.Tyr5090=
NM_020765.3:c.15260A= MANE Select	NP_065816.2:p.Tyr5087=