Canonical Allele Identifier: CA1156956079

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078025G= , CM000663.2:g.19078025G=	GRCh38
NC_000001.10:g.19404519G= , CM000663.1:g.19404519G=	GRCh37
NC_000001.9:g.19277106G=	NCBI36
NG_027669.1:g.137228C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15275C= MANE Select	ENSP00000364403.3:p.Ser5092=
ENST00000375224.1:c.2396C=	ENSP00000364372.1:p.Ser799=
ENST00000375225.7:c.500C=	ENSP00000364373.3:p.Ser167=
ENST00000375254.7:c.15275C=	ENSP00000364403.3:p.Ser5092=
ENST00000459947.5:n.3282C=
NM_020765.2:c.15275C=	NP_065816.2:p.Ser5092=
XM_011541108.1:c.15428C=	XP_011539410.1:p.Ser5143=
XM_011541109.1:c.15425C=	XP_011539411.1:p.Ser5142=
XM_011541110.1:c.15425C=	XP_011539412.1:p.Ser5142=
XM_011541111.1:c.15425C=	XP_011539413.1:p.Ser5142=
XM_011541112.1:c.15413C=	XP_011539414.1:p.Ser5138=
XM_011541113.1:c.15410C=	XP_011539415.1:p.Ser5137=
XM_011541114.1:c.15410C=	XP_011539416.1:p.Ser5137=
XM_011541115.1:c.15404C=	XP_011539417.1:p.Ser5135=
XM_011541116.1:c.15395C=	XP_011539418.1:p.Ser5132=
XM_011541117.1:c.15344C=	XP_011539419.1:p.Ser5115=
XM_011541118.1:c.15341C=	XP_011539420.1:p.Ser5114=
XM_011541119.1:c.15308C=	XP_011539421.1:p.Ser5103=
XM_011541120.1:c.15305C=	XP_011539422.1:p.Ser5102=
XM_011541121.1:c.15272C=	XP_011539423.1:p.Ser5091=
XM_011541108.3:c.15542C=	XP_011539410.2:p.Ser5181=
XM_011541109.3:c.15539C=	XP_011539411.2:p.Ser5180=
XM_011541110.3:c.15539C=	XP_011539412.2:p.Ser5180=
XM_011541111.3:c.15539C=	XP_011539413.2:p.Ser5180=
XM_011541112.3:c.15527C=	XP_011539414.2:p.Ser5176=
XM_011541113.3:c.15524C=	XP_011539415.2:p.Ser5175=
XM_011541114.3:c.15524C=	XP_011539416.2:p.Ser5175=
XM_011541115.3:c.15518C=	XP_011539417.2:p.Ser5173=
XM_011541116.3:c.15509C=	XP_011539418.2:p.Ser5170=
XM_011541117.3:c.15458C=	XP_011539419.2:p.Ser5153=
XM_011541118.3:c.15455C=	XP_011539420.2:p.Ser5152=
XM_011541119.3:c.15422C=	XP_011539421.2:p.Ser5141=
XM_011541120.3:c.15419C=	XP_011539422.2:p.Ser5140=
XM_011541121.3:c.15386C=	XP_011539423.2:p.Ser5129=
XM_017000822.2:c.15521C=	XP_016856311.2:p.Ser5174=
XM_017000823.2:c.15494C=	XP_016856312.2:p.Ser5165=
XM_017000824.2:c.15440C=	XP_016856313.2:p.Ser5147=
XM_017000825.2:c.15425C=	XP_016856314.2:p.Ser5142=
XM_017000826.2:c.15422C=	XP_016856315.2:p.Ser5141=
XM_017000827.2:c.15407C=	XP_016856316.2:p.Ser5136=
XM_017000828.2:c.15383C=	XP_016856317.2:p.Ser5128=
XM_017000829.2:c.15335C=	XP_016856318.2:p.Ser5112=
XM_017000830.2:c.15284C=	XP_016856319.2:p.Ser5095=
NM_020765.3:c.15275C= MANE Select	NP_065816.2:p.Ser5092=