Canonical Allele Identifier: CA1156956066

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077987T= , CM000663.2:g.19077987T=	GRCh38
NC_000001.10:g.19404481T= , CM000663.1:g.19404481T=	GRCh37
NC_000001.9:g.19277068T=	NCBI36
NG_027669.1:g.137266A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15313A= MANE Select	ENSP00000364403.3:p.Asn5105=
ENST00000375224.1:c.2434A=	ENSP00000364372.1:p.Asn812=
ENST00000375225.7:c.538A=	ENSP00000364373.3:p.Asn180=
ENST00000375254.7:c.15313A=	ENSP00000364403.3:p.Asn5105=
ENST00000459947.5:n.3320A=
NM_020765.2:c.15313A=	NP_065816.2:p.Asn5105=
XM_011541108.1:c.15466A=	XP_011539410.1:p.Asn5156=
XM_011541109.1:c.15463A=	XP_011539411.1:p.Asn5155=
XM_011541110.1:c.15463A=	XP_011539412.1:p.Asn5155=
XM_011541111.1:c.15463A=	XP_011539413.1:p.Asn5155=
XM_011541112.1:c.15451A=	XP_011539414.1:p.Asn5151=
XM_011541113.1:c.15448A=	XP_011539415.1:p.Asn5150=
XM_011541114.1:c.15448A=	XP_011539416.1:p.Asn5150=
XM_011541115.1:c.15442A=	XP_011539417.1:p.Asn5148=
XM_011541116.1:c.15433A=	XP_011539418.1:p.Asn5145=
XM_011541117.1:c.15382A=	XP_011539419.1:p.Asn5128=
XM_011541118.1:c.15379A=	XP_011539420.1:p.Asn5127=
XM_011541119.1:c.15346A=	XP_011539421.1:p.Asn5116=
XM_011541120.1:c.15343A=	XP_011539422.1:p.Asn5115=
XM_011541121.1:c.15310A=	XP_011539423.1:p.Asn5104=
XM_011541108.3:c.15580A=	XP_011539410.2:p.Asn5194=
XM_011541109.3:c.15577A=	XP_011539411.2:p.Asn5193=
XM_011541110.3:c.15577A=	XP_011539412.2:p.Asn5193=
XM_011541111.3:c.15577A=	XP_011539413.2:p.Asn5193=
XM_011541112.3:c.15565A=	XP_011539414.2:p.Asn5189=
XM_011541113.3:c.15562A=	XP_011539415.2:p.Asn5188=
XM_011541114.3:c.15562A=	XP_011539416.2:p.Asn5188=
XM_011541115.3:c.15556A=	XP_011539417.2:p.Asn5186=
XM_011541116.3:c.15547A=	XP_011539418.2:p.Asn5183=
XM_011541117.3:c.15496A=	XP_011539419.2:p.Asn5166=
XM_011541118.3:c.15493A=	XP_011539420.2:p.Asn5165=
XM_011541119.3:c.15460A=	XP_011539421.2:p.Asn5154=
XM_011541120.3:c.15457A=	XP_011539422.2:p.Asn5153=
XM_011541121.3:c.15424A=	XP_011539423.2:p.Asn5142=
XM_017000822.2:c.15559A=	XP_016856311.2:p.Asn5187=
XM_017000823.2:c.15532A=	XP_016856312.2:p.Asn5178=
XM_017000824.2:c.15478A=	XP_016856313.2:p.Asn5160=
XM_017000825.2:c.15463A=	XP_016856314.2:p.Asn5155=
XM_017000826.2:c.15460A=	XP_016856315.2:p.Asn5154=
XM_017000827.2:c.15445A=	XP_016856316.2:p.Asn5149=
XM_017000828.2:c.15421A=	XP_016856317.2:p.Asn5141=
XM_017000829.2:c.15373A=	XP_016856318.2:p.Asn5125=
XM_017000830.2:c.15322A=	XP_016856319.2:p.Asn5108=
NM_020765.3:c.15313A= MANE Select	NP_065816.2:p.Asn5105=