Canonical Allele Identifier: CA1156956067

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077989T= , CM000663.2:g.19077989T=	GRCh38
NC_000001.10:g.19404483T= , CM000663.1:g.19404483T=	GRCh37
NC_000001.9:g.19277070T=	NCBI36
NG_027669.1:g.137264A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15311A= MANE Select	ENSP00000364403.3:p.Tyr5104=
ENST00000375224.1:c.2432A=	ENSP00000364372.1:p.Tyr811=
ENST00000375225.7:c.536A=	ENSP00000364373.3:p.Tyr179=
ENST00000375254.7:c.15311A=	ENSP00000364403.3:p.Tyr5104=
ENST00000459947.5:n.3318A=
NM_020765.2:c.15311A=	NP_065816.2:p.Tyr5104=
XM_011541108.1:c.15464A=	XP_011539410.1:p.Tyr5155=
XM_011541109.1:c.15461A=	XP_011539411.1:p.Tyr5154=
XM_011541110.1:c.15461A=	XP_011539412.1:p.Tyr5154=
XM_011541111.1:c.15461A=	XP_011539413.1:p.Tyr5154=
XM_011541112.1:c.15449A=	XP_011539414.1:p.Tyr5150=
XM_011541113.1:c.15446A=	XP_011539415.1:p.Tyr5149=
XM_011541114.1:c.15446A=	XP_011539416.1:p.Tyr5149=
XM_011541115.1:c.15440A=	XP_011539417.1:p.Tyr5147=
XM_011541116.1:c.15431A=	XP_011539418.1:p.Tyr5144=
XM_011541117.1:c.15380A=	XP_011539419.1:p.Tyr5127=
XM_011541118.1:c.15377A=	XP_011539420.1:p.Tyr5126=
XM_011541119.1:c.15344A=	XP_011539421.1:p.Tyr5115=
XM_011541120.1:c.15341A=	XP_011539422.1:p.Tyr5114=
XM_011541121.1:c.15308A=	XP_011539423.1:p.Tyr5103=
XM_011541108.3:c.15578A=	XP_011539410.2:p.Tyr5193=
XM_011541109.3:c.15575A=	XP_011539411.2:p.Tyr5192=
XM_011541110.3:c.15575A=	XP_011539412.2:p.Tyr5192=
XM_011541111.3:c.15575A=	XP_011539413.2:p.Tyr5192=
XM_011541112.3:c.15563A=	XP_011539414.2:p.Tyr5188=
XM_011541113.3:c.15560A=	XP_011539415.2:p.Tyr5187=
XM_011541114.3:c.15560A=	XP_011539416.2:p.Tyr5187=
XM_011541115.3:c.15554A=	XP_011539417.2:p.Tyr5185=
XM_011541116.3:c.15545A=	XP_011539418.2:p.Tyr5182=
XM_011541117.3:c.15494A=	XP_011539419.2:p.Tyr5165=
XM_011541118.3:c.15491A=	XP_011539420.2:p.Tyr5164=
XM_011541119.3:c.15458A=	XP_011539421.2:p.Tyr5153=
XM_011541120.3:c.15455A=	XP_011539422.2:p.Tyr5152=
XM_011541121.3:c.15422A=	XP_011539423.2:p.Tyr5141=
XM_017000822.2:c.15557A=	XP_016856311.2:p.Tyr5186=
XM_017000823.2:c.15530A=	XP_016856312.2:p.Tyr5177=
XM_017000824.2:c.15476A=	XP_016856313.2:p.Tyr5159=
XM_017000825.2:c.15461A=	XP_016856314.2:p.Tyr5154=
XM_017000826.2:c.15458A=	XP_016856315.2:p.Tyr5153=
XM_017000827.2:c.15443A=	XP_016856316.2:p.Tyr5148=
XM_017000828.2:c.15419A=	XP_016856317.2:p.Tyr5140=
XM_017000829.2:c.15371A=	XP_016856318.2:p.Tyr5124=
XM_017000830.2:c.15320A=	XP_016856319.2:p.Tyr5107=
NM_020765.3:c.15311A= MANE Select	NP_065816.2:p.Tyr5104=