Canonical Allele Identifier: CA1156956065

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077984T= , CM000663.2:g.19077984T=	GRCh38
NC_000001.10:g.19404478T= , CM000663.1:g.19404478T=	GRCh37
NC_000001.9:g.19277065T=	NCBI36
NG_027669.1:g.137269A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15316A= MANE Select	ENSP00000364403.3:p.Met5106=
ENST00000375224.1:c.2437A=	ENSP00000364372.1:p.Met813=
ENST00000375225.7:c.541A=	ENSP00000364373.3:p.Met181=
ENST00000375254.7:c.15316A=	ENSP00000364403.3:p.Met5106=
ENST00000459947.5:n.3323A=
NM_020765.2:c.15316A=	NP_065816.2:p.Met5106=
XM_011541108.1:c.15469A=	XP_011539410.1:p.Met5157=
XM_011541109.1:c.15466A=	XP_011539411.1:p.Met5156=
XM_011541110.1:c.15466A=	XP_011539412.1:p.Met5156=
XM_011541111.1:c.15466A=	XP_011539413.1:p.Met5156=
XM_011541112.1:c.15454A=	XP_011539414.1:p.Met5152=
XM_011541113.1:c.15451A=	XP_011539415.1:p.Met5151=
XM_011541114.1:c.15451A=	XP_011539416.1:p.Met5151=
XM_011541115.1:c.15445A=	XP_011539417.1:p.Met5149=
XM_011541116.1:c.15436A=	XP_011539418.1:p.Met5146=
XM_011541117.1:c.15385A=	XP_011539419.1:p.Met5129=
XM_011541118.1:c.15382A=	XP_011539420.1:p.Met5128=
XM_011541119.1:c.15349A=	XP_011539421.1:p.Met5117=
XM_011541120.1:c.15346A=	XP_011539422.1:p.Met5116=
XM_011541121.1:c.15313A=	XP_011539423.1:p.Met5105=
XM_011541108.3:c.15583A=	XP_011539410.2:p.Met5195=
XM_011541109.3:c.15580A=	XP_011539411.2:p.Met5194=
XM_011541110.3:c.15580A=	XP_011539412.2:p.Met5194=
XM_011541111.3:c.15580A=	XP_011539413.2:p.Met5194=
XM_011541112.3:c.15568A=	XP_011539414.2:p.Met5190=
XM_011541113.3:c.15565A=	XP_011539415.2:p.Met5189=
XM_011541114.3:c.15565A=	XP_011539416.2:p.Met5189=
XM_011541115.3:c.15559A=	XP_011539417.2:p.Met5187=
XM_011541116.3:c.15550A=	XP_011539418.2:p.Met5184=
XM_011541117.3:c.15499A=	XP_011539419.2:p.Met5167=
XM_011541118.3:c.15496A=	XP_011539420.2:p.Met5166=
XM_011541119.3:c.15463A=	XP_011539421.2:p.Met5155=
XM_011541120.3:c.15460A=	XP_011539422.2:p.Met5154=
XM_011541121.3:c.15427A=	XP_011539423.2:p.Met5143=
XM_017000822.2:c.15562A=	XP_016856311.2:p.Met5188=
XM_017000823.2:c.15535A=	XP_016856312.2:p.Met5179=
XM_017000824.2:c.15481A=	XP_016856313.2:p.Met5161=
XM_017000825.2:c.15466A=	XP_016856314.2:p.Met5156=
XM_017000826.2:c.15463A=	XP_016856315.2:p.Met5155=
XM_017000827.2:c.15448A=	XP_016856316.2:p.Met5150=
XM_017000828.2:c.15424A=	XP_016856317.2:p.Met5142=
XM_017000829.2:c.15376A=	XP_016856318.2:p.Met5126=
XM_017000830.2:c.15325A=	XP_016856319.2:p.Met5109=
NM_020765.3:c.15316A= MANE Select	NP_065816.2:p.Met5106=