Canonical Allele Identifier: CA1156956068

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077990A= , CM000663.2:g.19077990A=	GRCh38
NC_000001.10:g.19404484A= , CM000663.1:g.19404484A=	GRCh37
NC_000001.9:g.19277071A=	NCBI36
NG_027669.1:g.137263T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15310T= MANE Select	ENSP00000364403.3:p.Tyr5104=
ENST00000375224.1:c.2431T=	ENSP00000364372.1:p.Tyr811=
ENST00000375225.7:c.535T=	ENSP00000364373.3:p.Tyr179=
ENST00000375254.7:c.15310T=	ENSP00000364403.3:p.Tyr5104=
ENST00000459947.5:n.3317T=
NM_020765.2:c.15310T=	NP_065816.2:p.Tyr5104=
XM_011541108.1:c.15463T=	XP_011539410.1:p.Tyr5155=
XM_011541109.1:c.15460T=	XP_011539411.1:p.Tyr5154=
XM_011541110.1:c.15460T=	XP_011539412.1:p.Tyr5154=
XM_011541111.1:c.15460T=	XP_011539413.1:p.Tyr5154=
XM_011541112.1:c.15448T=	XP_011539414.1:p.Tyr5150=
XM_011541113.1:c.15445T=	XP_011539415.1:p.Tyr5149=
XM_011541114.1:c.15445T=	XP_011539416.1:p.Tyr5149=
XM_011541115.1:c.15439T=	XP_011539417.1:p.Tyr5147=
XM_011541116.1:c.15430T=	XP_011539418.1:p.Tyr5144=
XM_011541117.1:c.15379T=	XP_011539419.1:p.Tyr5127=
XM_011541118.1:c.15376T=	XP_011539420.1:p.Tyr5126=
XM_011541119.1:c.15343T=	XP_011539421.1:p.Tyr5115=
XM_011541120.1:c.15340T=	XP_011539422.1:p.Tyr5114=
XM_011541121.1:c.15307T=	XP_011539423.1:p.Tyr5103=
XM_011541108.3:c.15577T=	XP_011539410.2:p.Tyr5193=
XM_011541109.3:c.15574T=	XP_011539411.2:p.Tyr5192=
XM_011541110.3:c.15574T=	XP_011539412.2:p.Tyr5192=
XM_011541111.3:c.15574T=	XP_011539413.2:p.Tyr5192=
XM_011541112.3:c.15562T=	XP_011539414.2:p.Tyr5188=
XM_011541113.3:c.15559T=	XP_011539415.2:p.Tyr5187=
XM_011541114.3:c.15559T=	XP_011539416.2:p.Tyr5187=
XM_011541115.3:c.15553T=	XP_011539417.2:p.Tyr5185=
XM_011541116.3:c.15544T=	XP_011539418.2:p.Tyr5182=
XM_011541117.3:c.15493T=	XP_011539419.2:p.Tyr5165=
XM_011541118.3:c.15490T=	XP_011539420.2:p.Tyr5164=
XM_011541119.3:c.15457T=	XP_011539421.2:p.Tyr5153=
XM_011541120.3:c.15454T=	XP_011539422.2:p.Tyr5152=
XM_011541121.3:c.15421T=	XP_011539423.2:p.Tyr5141=
XM_017000822.2:c.15556T=	XP_016856311.2:p.Tyr5186=
XM_017000823.2:c.15529T=	XP_016856312.2:p.Tyr5177=
XM_017000824.2:c.15475T=	XP_016856313.2:p.Tyr5159=
XM_017000825.2:c.15460T=	XP_016856314.2:p.Tyr5154=
XM_017000826.2:c.15457T=	XP_016856315.2:p.Tyr5153=
XM_017000827.2:c.15442T=	XP_016856316.2:p.Tyr5148=
XM_017000828.2:c.15418T=	XP_016856317.2:p.Tyr5140=
XM_017000829.2:c.15370T=	XP_016856318.2:p.Tyr5124=
XM_017000830.2:c.15319T=	XP_016856319.2:p.Tyr5107=
NM_020765.3:c.15310T= MANE Select	NP_065816.2:p.Tyr5104=