Canonical Allele Identifier: CA1156956084

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078036G= , CM000663.2:g.19078036G=	GRCh38
NC_000001.10:g.19404530G= , CM000663.1:g.19404530G=	GRCh37
NC_000001.9:g.19277117G=	NCBI36
NG_027669.1:g.137217C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15264C= MANE Select	ENSP00000364403.3:p.Ser5088=
ENST00000375224.1:c.2385C=	ENSP00000364372.1:p.Ser795=
ENST00000375225.7:c.489C=	ENSP00000364373.3:p.Ser163=
ENST00000375254.7:c.15264C=	ENSP00000364403.3:p.Ser5088=
ENST00000459947.5:n.3271C=
NM_020765.2:c.15264C=	NP_065816.2:p.Ser5088=
XM_011541108.1:c.15417C=	XP_011539410.1:p.Ser5139=
XM_011541109.1:c.15414C=	XP_011539411.1:p.Ser5138=
XM_011541110.1:c.15414C=	XP_011539412.1:p.Ser5138=
XM_011541111.1:c.15414C=	XP_011539413.1:p.Ser5138=
XM_011541112.1:c.15402C=	XP_011539414.1:p.Ser5134=
XM_011541113.1:c.15399C=	XP_011539415.1:p.Ser5133=
XM_011541114.1:c.15399C=	XP_011539416.1:p.Ser5133=
XM_011541115.1:c.15393C=	XP_011539417.1:p.Ser5131=
XM_011541116.1:c.15384C=	XP_011539418.1:p.Ser5128=
XM_011541117.1:c.15333C=	XP_011539419.1:p.Ser5111=
XM_011541118.1:c.15330C=	XP_011539420.1:p.Ser5110=
XM_011541119.1:c.15297C=	XP_011539421.1:p.Ser5099=
XM_011541120.1:c.15294C=	XP_011539422.1:p.Ser5098=
XM_011541121.1:c.15261C=	XP_011539423.1:p.Ser5087=
XM_011541108.3:c.15531C=	XP_011539410.2:p.Ser5177=
XM_011541109.3:c.15528C=	XP_011539411.2:p.Ser5176=
XM_011541110.3:c.15528C=	XP_011539412.2:p.Ser5176=
XM_011541111.3:c.15528C=	XP_011539413.2:p.Ser5176=
XM_011541112.3:c.15516C=	XP_011539414.2:p.Ser5172=
XM_011541113.3:c.15513C=	XP_011539415.2:p.Ser5171=
XM_011541114.3:c.15513C=	XP_011539416.2:p.Ser5171=
XM_011541115.3:c.15507C=	XP_011539417.2:p.Ser5169=
XM_011541116.3:c.15498C=	XP_011539418.2:p.Ser5166=
XM_011541117.3:c.15447C=	XP_011539419.2:p.Ser5149=
XM_011541118.3:c.15444C=	XP_011539420.2:p.Ser5148=
XM_011541119.3:c.15411C=	XP_011539421.2:p.Ser5137=
XM_011541120.3:c.15408C=	XP_011539422.2:p.Ser5136=
XM_011541121.3:c.15375C=	XP_011539423.2:p.Ser5125=
XM_017000822.2:c.15510C=	XP_016856311.2:p.Ser5170=
XM_017000823.2:c.15483C=	XP_016856312.2:p.Ser5161=
XM_017000824.2:c.15429C=	XP_016856313.2:p.Ser5143=
XM_017000825.2:c.15414C=	XP_016856314.2:p.Ser5138=
XM_017000826.2:c.15411C=	XP_016856315.2:p.Ser5137=
XM_017000827.2:c.15396C=	XP_016856316.2:p.Ser5132=
XM_017000828.2:c.15372C=	XP_016856317.2:p.Ser5124=
XM_017000829.2:c.15324C=	XP_016856318.2:p.Ser5108=
XM_017000830.2:c.15273C=	XP_016856319.2:p.Ser5091=
NM_020765.3:c.15264C= MANE Select	NP_065816.2:p.Ser5088=