Canonical Allele Identifier: CA1139925417

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078050C= , CM000663.2:g.19078050C=	GRCh38
NC_000001.10:g.19404544C= , CM000663.1:g.19404544C=	GRCh37
NC_000001.9:g.19277131C=	NCBI36
NG_027669.1:g.137203G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15250G= MANE Select	ENSP00000364403.3:p.Val5084=
ENST00000375224.1:c.2371G=	ENSP00000364372.1:p.Val791=
ENST00000375225.7:c.475G=	ENSP00000364373.3:p.Val159=
ENST00000375254.7:c.15250G=	ENSP00000364403.3:p.Val5084=
ENST00000459947.5:n.3257G=
NM_020765.2:c.15250G=	NP_065816.2:p.Val5084=
XM_011541108.1:c.15403G=	XP_011539410.1:p.Val5135=
XM_011541109.1:c.15400G=	XP_011539411.1:p.Val5134=
XM_011541110.1:c.15400G=	XP_011539412.1:p.Val5134=
XM_011541111.1:c.15400G=	XP_011539413.1:p.Val5134=
XM_011541112.1:c.15388G=	XP_011539414.1:p.Val5130=
XM_011541113.1:c.15385G=	XP_011539415.1:p.Val5129=
XM_011541114.1:c.15385G=	XP_011539416.1:p.Val5129=
XM_011541115.1:c.15379G=	XP_011539417.1:p.Val5127=
XM_011541116.1:c.15370G=	XP_011539418.1:p.Val5124=
XM_011541117.1:c.15319G=	XP_011539419.1:p.Val5107=
XM_011541118.1:c.15316G=	XP_011539420.1:p.Val5106=
XM_011541119.1:c.15283G=	XP_011539421.1:p.Val5095=
XM_011541120.1:c.15280G=	XP_011539422.1:p.Val5094=
XM_011541121.1:c.15247G=	XP_011539423.1:p.Val5083=
XM_011541108.3:c.15517G=	XP_011539410.2:p.Val5173=
XM_011541109.3:c.15514G=	XP_011539411.2:p.Val5172=
XM_011541110.3:c.15514G=	XP_011539412.2:p.Val5172=
XM_011541111.3:c.15514G=	XP_011539413.2:p.Val5172=
XM_011541112.3:c.15502G=	XP_011539414.2:p.Val5168=
XM_011541113.3:c.15499G=	XP_011539415.2:p.Val5167=
XM_011541114.3:c.15499G=	XP_011539416.2:p.Val5167=
XM_011541115.3:c.15493G=	XP_011539417.2:p.Val5165=
XM_011541116.3:c.15484G=	XP_011539418.2:p.Val5162=
XM_011541117.3:c.15433G=	XP_011539419.2:p.Val5145=
XM_011541118.3:c.15430G=	XP_011539420.2:p.Val5144=
XM_011541119.3:c.15397G=	XP_011539421.2:p.Val5133=
XM_011541120.3:c.15394G=	XP_011539422.2:p.Val5132=
XM_011541121.3:c.15361G=	XP_011539423.2:p.Val5121=
XM_017000822.2:c.15496G=	XP_016856311.2:p.Val5166=
XM_017000823.2:c.15469G=	XP_016856312.2:p.Val5157=
XM_017000824.2:c.15415G=	XP_016856313.2:p.Val5139=
XM_017000825.2:c.15400G=	XP_016856314.2:p.Val5134=
XM_017000826.2:c.15397G=	XP_016856315.2:p.Val5133=
XM_017000827.2:c.15382G=	XP_016856316.2:p.Val5128=
XM_017000828.2:c.15358G=	XP_016856317.2:p.Val5120=
XM_017000829.2:c.15310G=	XP_016856318.2:p.Val5104=
XM_017000830.2:c.15259G=	XP_016856319.2:p.Val5087=
NM_020765.3:c.15250G= MANE Select	NP_065816.2:p.Val5084=