Canonical Allele Identifier: CA1156956064

Gene: UBR4

Linked Data

• dbSNP Id: rs2076123979
• gnomAD v4: 1-19077983-ATGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077987_19077989del , CM000663.2:g.19077987_19077989del	GRCh38
NC_000001.10:g.19404481_19404483del , CM000663.1:g.19404481_19404483del	GRCh37
NC_000001.9:g.19277068_19277070del	NCBI36
NG_027669.1:g.137267_137269del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15314_15316del MANE Select	ENSP00000364403.3:p.Asn5105del
ENST00000375224.1:c.2435_2437del	ENSP00000364372.1:p.Asn812del
ENST00000375225.7:c.539_541del	ENSP00000364373.3:p.Asn180del
ENST00000375254.7:c.15314_15316del	ENSP00000364403.3:p.Asn5105del
ENST00000459947.5:n.3321_3323del
NM_020765.2:c.15314_15316del	NP_065816.2:p.Asn5105del
XM_011541108.1:c.15467_15469del	XP_011539410.1:p.Asn5156del
XM_011541109.1:c.15464_15466del	XP_011539411.1:p.Asn5155del
XM_011541110.1:c.15464_15466del	XP_011539412.1:p.Asn5155del
XM_011541111.1:c.15464_15466del	XP_011539413.1:p.Asn5155del
XM_011541112.1:c.15452_15454del	XP_011539414.1:p.Asn5151del
XM_011541113.1:c.15449_15451del	XP_011539415.1:p.Asn5150del
XM_011541114.1:c.15449_15451del	XP_011539416.1:p.Asn5150del
XM_011541115.1:c.15443_15445del	XP_011539417.1:p.Asn5148del
XM_011541116.1:c.15434_15436del	XP_011539418.1:p.Asn5145del
XM_011541117.1:c.15383_15385del	XP_011539419.1:p.Asn5128del
XM_011541118.1:c.15380_15382del	XP_011539420.1:p.Asn5127del
XM_011541119.1:c.15347_15349del	XP_011539421.1:p.Asn5116del
XM_011541120.1:c.15344_15346del	XP_011539422.1:p.Asn5115del
XM_011541121.1:c.15311_15313del	XP_011539423.1:p.Asn5104del
XM_011541108.3:c.15581_15583del	XP_011539410.2:p.Asn5194del
XM_011541109.3:c.15578_15580del	XP_011539411.2:p.Asn5193del
XM_011541110.3:c.15578_15580del	XP_011539412.2:p.Asn5193del
XM_011541111.3:c.15578_15580del	XP_011539413.2:p.Asn5193del
XM_011541112.3:c.15566_15568del	XP_011539414.2:p.Asn5189del
XM_011541113.3:c.15563_15565del	XP_011539415.2:p.Asn5188del
XM_011541114.3:c.15563_15565del	XP_011539416.2:p.Asn5188del
XM_011541115.3:c.15557_15559del	XP_011539417.2:p.Asn5186del
XM_011541116.3:c.15548_15550del	XP_011539418.2:p.Asn5183del
XM_011541117.3:c.15497_15499del	XP_011539419.2:p.Asn5166del
XM_011541118.3:c.15494_15496del	XP_011539420.2:p.Asn5165del
XM_011541119.3:c.15461_15463del	XP_011539421.2:p.Asn5154del
XM_011541120.3:c.15458_15460del	XP_011539422.2:p.Asn5153del
XM_011541121.3:c.15425_15427del	XP_011539423.2:p.Asn5142del
XM_017000822.2:c.15560_15562del	XP_016856311.2:p.Asn5187del
XM_017000823.2:c.15533_15535del	XP_016856312.2:p.Asn5178del
XM_017000824.2:c.15479_15481del	XP_016856313.2:p.Asn5160del
XM_017000825.2:c.15464_15466del	XP_016856314.2:p.Asn5155del
XM_017000826.2:c.15461_15463del	XP_016856315.2:p.Asn5154del
XM_017000827.2:c.15446_15448del	XP_016856316.2:p.Asn5149del
XM_017000828.2:c.15422_15424del	XP_016856317.2:p.Asn5141del
XM_017000829.2:c.15374_15376del	XP_016856318.2:p.Asn5125del
XM_017000830.2:c.15323_15325del	XP_016856319.2:p.Asn5108del
NM_020765.3:c.15314_15316del MANE Select	NP_065816.2:p.Asn5105del