Canonical Allele Identifier: CA1141706695

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077986T= , CM000663.2:g.19077986T=	GRCh38
NC_000001.10:g.19404480T= , CM000663.1:g.19404480T=	GRCh37
NC_000001.9:g.19277067T=	NCBI36
NG_027669.1:g.137267A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15314A= MANE Select	ENSP00000364403.3:p.Asn5105=
ENST00000375224.1:c.2435A=	ENSP00000364372.1:p.Asn812=
ENST00000375225.7:c.539A=	ENSP00000364373.3:p.Asn180=
ENST00000375254.7:c.15314A=	ENSP00000364403.3:p.Asn5105=
ENST00000459947.5:n.3321A=
NM_020765.2:c.15314A=	NP_065816.2:p.Asn5105=
XM_011541108.1:c.15467A=	XP_011539410.1:p.Asn5156=
XM_011541109.1:c.15464A=	XP_011539411.1:p.Asn5155=
XM_011541110.1:c.15464A=	XP_011539412.1:p.Asn5155=
XM_011541111.1:c.15464A=	XP_011539413.1:p.Asn5155=
XM_011541112.1:c.15452A=	XP_011539414.1:p.Asn5151=
XM_011541113.1:c.15449A=	XP_011539415.1:p.Asn5150=
XM_011541114.1:c.15449A=	XP_011539416.1:p.Asn5150=
XM_011541115.1:c.15443A=	XP_011539417.1:p.Asn5148=
XM_011541116.1:c.15434A=	XP_011539418.1:p.Asn5145=
XM_011541117.1:c.15383A=	XP_011539419.1:p.Asn5128=
XM_011541118.1:c.15380A=	XP_011539420.1:p.Asn5127=
XM_011541119.1:c.15347A=	XP_011539421.1:p.Asn5116=
XM_011541120.1:c.15344A=	XP_011539422.1:p.Asn5115=
XM_011541121.1:c.15311A=	XP_011539423.1:p.Asn5104=
XM_011541108.3:c.15581A=	XP_011539410.2:p.Asn5194=
XM_011541109.3:c.15578A=	XP_011539411.2:p.Asn5193=
XM_011541110.3:c.15578A=	XP_011539412.2:p.Asn5193=
XM_011541111.3:c.15578A=	XP_011539413.2:p.Asn5193=
XM_011541112.3:c.15566A=	XP_011539414.2:p.Asn5189=
XM_011541113.3:c.15563A=	XP_011539415.2:p.Asn5188=
XM_011541114.3:c.15563A=	XP_011539416.2:p.Asn5188=
XM_011541115.3:c.15557A=	XP_011539417.2:p.Asn5186=
XM_011541116.3:c.15548A=	XP_011539418.2:p.Asn5183=
XM_011541117.3:c.15497A=	XP_011539419.2:p.Asn5166=
XM_011541118.3:c.15494A=	XP_011539420.2:p.Asn5165=
XM_011541119.3:c.15461A=	XP_011539421.2:p.Asn5154=
XM_011541120.3:c.15458A=	XP_011539422.2:p.Asn5153=
XM_011541121.3:c.15425A=	XP_011539423.2:p.Asn5142=
XM_017000822.2:c.15560A=	XP_016856311.2:p.Asn5187=
XM_017000823.2:c.15533A=	XP_016856312.2:p.Asn5178=
XM_017000824.2:c.15479A=	XP_016856313.2:p.Asn5160=
XM_017000825.2:c.15464A=	XP_016856314.2:p.Asn5155=
XM_017000826.2:c.15461A=	XP_016856315.2:p.Asn5154=
XM_017000827.2:c.15446A=	XP_016856316.2:p.Asn5149=
XM_017000828.2:c.15422A=	XP_016856317.2:p.Asn5141=
XM_017000829.2:c.15374A=	XP_016856318.2:p.Asn5125=
XM_017000830.2:c.15323A=	XP_016856319.2:p.Asn5108=
NM_020765.3:c.15314A= MANE Select	NP_065816.2:p.Asn5105=