Canonical Allele Identifier: CA1156956070

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077996G= , CM000663.2:g.19077996G=	GRCh38
NC_000001.10:g.19404490G= , CM000663.1:g.19404490G=	GRCh37
NC_000001.9:g.19277077G=	NCBI36
NG_027669.1:g.137257C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15304C= MANE Select	ENSP00000364403.3:p.Leu5102=
ENST00000375224.1:c.2425C=	ENSP00000364372.1:p.Leu809=
ENST00000375225.7:c.529C=	ENSP00000364373.3:p.Leu177=
ENST00000375254.7:c.15304C=	ENSP00000364403.3:p.Leu5102=
ENST00000459947.5:n.3311C=
NM_020765.2:c.15304C=	NP_065816.2:p.Leu5102=
XM_011541108.1:c.15457C=	XP_011539410.1:p.Leu5153=
XM_011541109.1:c.15454C=	XP_011539411.1:p.Leu5152=
XM_011541110.1:c.15454C=	XP_011539412.1:p.Leu5152=
XM_011541111.1:c.15454C=	XP_011539413.1:p.Leu5152=
XM_011541112.1:c.15442C=	XP_011539414.1:p.Leu5148=
XM_011541113.1:c.15439C=	XP_011539415.1:p.Leu5147=
XM_011541114.1:c.15439C=	XP_011539416.1:p.Leu5147=
XM_011541115.1:c.15433C=	XP_011539417.1:p.Leu5145=
XM_011541116.1:c.15424C=	XP_011539418.1:p.Leu5142=
XM_011541117.1:c.15373C=	XP_011539419.1:p.Leu5125=
XM_011541118.1:c.15370C=	XP_011539420.1:p.Leu5124=
XM_011541119.1:c.15337C=	XP_011539421.1:p.Leu5113=
XM_011541120.1:c.15334C=	XP_011539422.1:p.Leu5112=
XM_011541121.1:c.15301C=	XP_011539423.1:p.Leu5101=
XM_011541108.3:c.15571C=	XP_011539410.2:p.Leu5191=
XM_011541109.3:c.15568C=	XP_011539411.2:p.Leu5190=
XM_011541110.3:c.15568C=	XP_011539412.2:p.Leu5190=
XM_011541111.3:c.15568C=	XP_011539413.2:p.Leu5190=
XM_011541112.3:c.15556C=	XP_011539414.2:p.Leu5186=
XM_011541113.3:c.15553C=	XP_011539415.2:p.Leu5185=
XM_011541114.3:c.15553C=	XP_011539416.2:p.Leu5185=
XM_011541115.3:c.15547C=	XP_011539417.2:p.Leu5183=
XM_011541116.3:c.15538C=	XP_011539418.2:p.Leu5180=
XM_011541117.3:c.15487C=	XP_011539419.2:p.Leu5163=
XM_011541118.3:c.15484C=	XP_011539420.2:p.Leu5162=
XM_011541119.3:c.15451C=	XP_011539421.2:p.Leu5151=
XM_011541120.3:c.15448C=	XP_011539422.2:p.Leu5150=
XM_011541121.3:c.15415C=	XP_011539423.2:p.Leu5139=
XM_017000822.2:c.15550C=	XP_016856311.2:p.Leu5184=
XM_017000823.2:c.15523C=	XP_016856312.2:p.Leu5175=
XM_017000824.2:c.15469C=	XP_016856313.2:p.Leu5157=
XM_017000825.2:c.15454C=	XP_016856314.2:p.Leu5152=
XM_017000826.2:c.15451C=	XP_016856315.2:p.Leu5151=
XM_017000827.2:c.15436C=	XP_016856316.2:p.Leu5146=
XM_017000828.2:c.15412C=	XP_016856317.2:p.Leu5138=
XM_017000829.2:c.15364C=	XP_016856318.2:p.Leu5122=
XM_017000830.2:c.15313C=	XP_016856319.2:p.Leu5105=
NM_020765.3:c.15304C= MANE Select	NP_065816.2:p.Leu5102=