Canonical Allele Identifier: CA1156956075

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078007G= , CM000663.2:g.19078007G=	GRCh38
NC_000001.10:g.19404501G= , CM000663.1:g.19404501G=	GRCh37
NC_000001.9:g.19277088G=	NCBI36
NG_027669.1:g.137246C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15293C= MANE Select	ENSP00000364403.3:p.Ala5098=
ENST00000375224.1:c.2414C=	ENSP00000364372.1:p.Ala805=
ENST00000375225.7:c.518C=	ENSP00000364373.3:p.Ala173=
ENST00000375254.7:c.15293C=	ENSP00000364403.3:p.Ala5098=
ENST00000459947.5:n.3300C=
NM_020765.2:c.15293C=	NP_065816.2:p.Ala5098=
XM_011541108.1:c.15446C=	XP_011539410.1:p.Ala5149=
XM_011541109.1:c.15443C=	XP_011539411.1:p.Ala5148=
XM_011541110.1:c.15443C=	XP_011539412.1:p.Ala5148=
XM_011541111.1:c.15443C=	XP_011539413.1:p.Ala5148=
XM_011541112.1:c.15431C=	XP_011539414.1:p.Ala5144=
XM_011541113.1:c.15428C=	XP_011539415.1:p.Ala5143=
XM_011541114.1:c.15428C=	XP_011539416.1:p.Ala5143=
XM_011541115.1:c.15422C=	XP_011539417.1:p.Ala5141=
XM_011541116.1:c.15413C=	XP_011539418.1:p.Ala5138=
XM_011541117.1:c.15362C=	XP_011539419.1:p.Ala5121=
XM_011541118.1:c.15359C=	XP_011539420.1:p.Ala5120=
XM_011541119.1:c.15326C=	XP_011539421.1:p.Ala5109=
XM_011541120.1:c.15323C=	XP_011539422.1:p.Ala5108=
XM_011541121.1:c.15290C=	XP_011539423.1:p.Ala5097=
XM_011541108.3:c.15560C=	XP_011539410.2:p.Ala5187=
XM_011541109.3:c.15557C=	XP_011539411.2:p.Ala5186=
XM_011541110.3:c.15557C=	XP_011539412.2:p.Ala5186=
XM_011541111.3:c.15557C=	XP_011539413.2:p.Ala5186=
XM_011541112.3:c.15545C=	XP_011539414.2:p.Ala5182=
XM_011541113.3:c.15542C=	XP_011539415.2:p.Ala5181=
XM_011541114.3:c.15542C=	XP_011539416.2:p.Ala5181=
XM_011541115.3:c.15536C=	XP_011539417.2:p.Ala5179=
XM_011541116.3:c.15527C=	XP_011539418.2:p.Ala5176=
XM_011541117.3:c.15476C=	XP_011539419.2:p.Ala5159=
XM_011541118.3:c.15473C=	XP_011539420.2:p.Ala5158=
XM_011541119.3:c.15440C=	XP_011539421.2:p.Ala5147=
XM_011541120.3:c.15437C=	XP_011539422.2:p.Ala5146=
XM_011541121.3:c.15404C=	XP_011539423.2:p.Ala5135=
XM_017000822.2:c.15539C=	XP_016856311.2:p.Ala5180=
XM_017000823.2:c.15512C=	XP_016856312.2:p.Ala5171=
XM_017000824.2:c.15458C=	XP_016856313.2:p.Ala5153=
XM_017000825.2:c.15443C=	XP_016856314.2:p.Ala5148=
XM_017000826.2:c.15440C=	XP_016856315.2:p.Ala5147=
XM_017000827.2:c.15425C=	XP_016856316.2:p.Ala5142=
XM_017000828.2:c.15401C=	XP_016856317.2:p.Ala5134=
XM_017000829.2:c.15353C=	XP_016856318.2:p.Ala5118=
XM_017000830.2:c.15302C=	XP_016856319.2:p.Ala5101=
NM_020765.3:c.15293C= MANE Select	NP_065816.2:p.Ala5098=