Canonical Allele Identifier: CA1156956069

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077993T= , CM000663.2:g.19077993T=	GRCh38
NC_000001.10:g.19404487T= , CM000663.1:g.19404487T=	GRCh37
NC_000001.9:g.19277074T=	NCBI36
NG_027669.1:g.137260A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15307A= MANE Select	ENSP00000364403.3:p.Ile5103=
ENST00000375224.1:c.2428A=	ENSP00000364372.1:p.Ile810=
ENST00000375225.7:c.532A=	ENSP00000364373.3:p.Ile178=
ENST00000375254.7:c.15307A=	ENSP00000364403.3:p.Ile5103=
ENST00000459947.5:n.3314A=
NM_020765.2:c.15307A=	NP_065816.2:p.Ile5103=
XM_011541108.1:c.15460A=	XP_011539410.1:p.Ile5154=
XM_011541109.1:c.15457A=	XP_011539411.1:p.Ile5153=
XM_011541110.1:c.15457A=	XP_011539412.1:p.Ile5153=
XM_011541111.1:c.15457A=	XP_011539413.1:p.Ile5153=
XM_011541112.1:c.15445A=	XP_011539414.1:p.Ile5149=
XM_011541113.1:c.15442A=	XP_011539415.1:p.Ile5148=
XM_011541114.1:c.15442A=	XP_011539416.1:p.Ile5148=
XM_011541115.1:c.15436A=	XP_011539417.1:p.Ile5146=
XM_011541116.1:c.15427A=	XP_011539418.1:p.Ile5143=
XM_011541117.1:c.15376A=	XP_011539419.1:p.Ile5126=
XM_011541118.1:c.15373A=	XP_011539420.1:p.Ile5125=
XM_011541119.1:c.15340A=	XP_011539421.1:p.Ile5114=
XM_011541120.1:c.15337A=	XP_011539422.1:p.Ile5113=
XM_011541121.1:c.15304A=	XP_011539423.1:p.Ile5102=
XM_011541108.3:c.15574A=	XP_011539410.2:p.Ile5192=
XM_011541109.3:c.15571A=	XP_011539411.2:p.Ile5191=
XM_011541110.3:c.15571A=	XP_011539412.2:p.Ile5191=
XM_011541111.3:c.15571A=	XP_011539413.2:p.Ile5191=
XM_011541112.3:c.15559A=	XP_011539414.2:p.Ile5187=
XM_011541113.3:c.15556A=	XP_011539415.2:p.Ile5186=
XM_011541114.3:c.15556A=	XP_011539416.2:p.Ile5186=
XM_011541115.3:c.15550A=	XP_011539417.2:p.Ile5184=
XM_011541116.3:c.15541A=	XP_011539418.2:p.Ile5181=
XM_011541117.3:c.15490A=	XP_011539419.2:p.Ile5164=
XM_011541118.3:c.15487A=	XP_011539420.2:p.Ile5163=
XM_011541119.3:c.15454A=	XP_011539421.2:p.Ile5152=
XM_011541120.3:c.15451A=	XP_011539422.2:p.Ile5151=
XM_011541121.3:c.15418A=	XP_011539423.2:p.Ile5140=
XM_017000822.2:c.15553A=	XP_016856311.2:p.Ile5185=
XM_017000823.2:c.15526A=	XP_016856312.2:p.Ile5176=
XM_017000824.2:c.15472A=	XP_016856313.2:p.Ile5158=
XM_017000825.2:c.15457A=	XP_016856314.2:p.Ile5153=
XM_017000826.2:c.15454A=	XP_016856315.2:p.Ile5152=
XM_017000827.2:c.15439A=	XP_016856316.2:p.Ile5147=
XM_017000828.2:c.15415A=	XP_016856317.2:p.Ile5139=
XM_017000829.2:c.15367A=	XP_016856318.2:p.Ile5123=
XM_017000830.2:c.15316A=	XP_016856319.2:p.Ile5106=
NM_020765.3:c.15307A= MANE Select	NP_065816.2:p.Ile5103=