Canonical Allele Identifier: CA1156956062
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077983_19077986delinsATGT , CM000663.2:g.19077983_19077986delinsATGT GRCh38
NC_000001.10:g.19404477_19404480delinsATGT , CM000663.1:g.19404477_19404480delinsATGT GRCh37
NC_000001.9:g.19277064_19277067delinsATGT NCBI36
NG_027669.1:g.137267_137270delinsACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15314_15317delinsACAT MANE Select ENSP00000364403.3:p.Asn5105=
ENST00000375224.1:c.2435_2438delinsACAT ENSP00000364372.1:p.Asn812=
ENST00000375225.7:c.539_542delinsACAT ENSP00000364373.3:p.Asn180=
ENST00000375254.7:c.15314_15317delinsACAT ENSP00000364403.3:p.Asn5105=
ENST00000459947.5:n.3321_3324delinsACAT
NM_020765.2:c.15314_15317delinsACAT NP_065816.2:p.Asn5105=
XM_011541108.1:c.15467_15470delinsACAT XP_011539410.1:p.Asn5156=
XM_011541109.1:c.15464_15467delinsACAT XP_011539411.1:p.Asn5155=
XM_011541110.1:c.15464_15467delinsACAT XP_011539412.1:p.Asn5155=
XM_011541111.1:c.15464_15467delinsACAT XP_011539413.1:p.Asn5155=
XM_011541112.1:c.15452_15455delinsACAT XP_011539414.1:p.Asn5151=
XM_011541113.1:c.15449_15452delinsACAT XP_011539415.1:p.Asn5150=
XM_011541114.1:c.15449_15452delinsACAT XP_011539416.1:p.Asn5150=
XM_011541115.1:c.15443_15446delinsACAT XP_011539417.1:p.Asn5148=
XM_011541116.1:c.15434_15437delinsACAT XP_011539418.1:p.Asn5145=
XM_011541117.1:c.15383_15386delinsACAT XP_011539419.1:p.Asn5128=
XM_011541118.1:c.15380_15383delinsACAT XP_011539420.1:p.Asn5127=
XM_011541119.1:c.15347_15350delinsACAT XP_011539421.1:p.Asn5116=
XM_011541120.1:c.15344_15347delinsACAT XP_011539422.1:p.Asn5115=
XM_011541121.1:c.15311_15314delinsACAT XP_011539423.1:p.Asn5104=
XM_011541108.3:c.15581_15584delinsACAT XP_011539410.2:p.Asn5194=
XM_011541109.3:c.15578_15581delinsACAT XP_011539411.2:p.Asn5193=
XM_011541110.3:c.15578_15581delinsACAT XP_011539412.2:p.Asn5193=
XM_011541111.3:c.15578_15581delinsACAT XP_011539413.2:p.Asn5193=
XM_011541112.3:c.15566_15569delinsACAT XP_011539414.2:p.Asn5189=
XM_011541113.3:c.15563_15566delinsACAT XP_011539415.2:p.Asn5188=
XM_011541114.3:c.15563_15566delinsACAT XP_011539416.2:p.Asn5188=
XM_011541115.3:c.15557_15560delinsACAT XP_011539417.2:p.Asn5186=
XM_011541116.3:c.15548_15551delinsACAT XP_011539418.2:p.Asn5183=
XM_011541117.3:c.15497_15500delinsACAT XP_011539419.2:p.Asn5166=
XM_011541118.3:c.15494_15497delinsACAT XP_011539420.2:p.Asn5165=
XM_011541119.3:c.15461_15464delinsACAT XP_011539421.2:p.Asn5154=
XM_011541120.3:c.15458_15461delinsACAT XP_011539422.2:p.Asn5153=
XM_011541121.3:c.15425_15428delinsACAT XP_011539423.2:p.Asn5142=
XM_017000822.2:c.15560_15563delinsACAT XP_016856311.2:p.Asn5187=
XM_017000823.2:c.15533_15536delinsACAT XP_016856312.2:p.Asn5178=
XM_017000824.2:c.15479_15482delinsACAT XP_016856313.2:p.Asn5160=
XM_017000825.2:c.15464_15467delinsACAT XP_016856314.2:p.Asn5155=
XM_017000826.2:c.15461_15464delinsACAT XP_016856315.2:p.Asn5154=
XM_017000827.2:c.15446_15449delinsACAT XP_016856316.2:p.Asn5149=
XM_017000828.2:c.15422_15425delinsACAT XP_016856317.2:p.Asn5141=
XM_017000829.2:c.15374_15377delinsACAT XP_016856318.2:p.Asn5125=
XM_017000830.2:c.15323_15326delinsACAT XP_016856319.2:p.Asn5108=
NM_020765.3:c.15314_15317delinsACAT MANE Select NP_065816.2:p.Asn5105=