Canonical Allele Identifier: CA1156955956
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19077742_19077743delinsCA , CM000663.2:g.19077742_19077743delinsCA GRCh38
NC_000001.10:g.19404236_19404237delinsCA , CM000663.1:g.19404236_19404237delinsCA GRCh37
NC_000001.9:g.19276823_19276824delinsCA NCBI36
NG_027669.1:g.137510_137511delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15324+233_15324+234delinsTG MANE Select ENSP00000364403.3:n.15324+233_15324+234delinsTG
ENST00000375224.1:c.2445+233_2445+234delinsTG ENSP00000364372.1:n.2445+233_2445+234delinsTG
ENST00000375225.7:c.549+233_549+234delinsTG ENSP00000364373.3:n.549+233_549+234delinsTG
ENST00000375254.7:c.15324+233_15324+234delinsTG ENSP00000364403.3:n.15324+233_15324+234delinsTG
ENST00000459947.5:n.3331+233_3331+234delinsTG
ENST00000486515.1:n.43+42_43+43delinsTG
NM_020765.2:c.15324+233_15324+234delinsTG NP_065816.2:n.15324+233_15324+234delinsTG
XM_011541108.1:c.15477+233_15477+234delinsTG XP_011539410.1:n.15477+233_15477+234delinsTG
XM_011541109.1:c.15474+233_15474+234delinsTG XP_011539411.1:n.15474+233_15474+234delinsTG
XM_011541110.1:c.15474+233_15474+234delinsTG XP_011539412.1:n.15474+233_15474+234delinsTG
XM_011541111.1:c.15474+233_15474+234delinsTG XP_011539413.1:n.15474+233_15474+234delinsTG
XM_011541112.1:c.15462+233_15462+234delinsTG XP_011539414.1:n.15462+233_15462+234delinsTG
XM_011541113.1:c.15459+233_15459+234delinsTG XP_011539415.1:n.15459+233_15459+234delinsTG
XM_011541114.1:c.15459+233_15459+234delinsTG XP_011539416.1:n.15459+233_15459+234delinsTG
XM_011541115.1:c.15453+233_15453+234delinsTG XP_011539417.1:n.15453+233_15453+234delinsTG
XM_011541116.1:c.15444+233_15444+234delinsTG XP_011539418.1:n.15444+233_15444+234delinsTG
XM_011541117.1:c.15393+233_15393+234delinsTG XP_011539419.1:n.15393+233_15393+234delinsTG
XM_011541118.1:c.15390+233_15390+234delinsTG XP_011539420.1:n.15390+233_15390+234delinsTG
XM_011541119.1:c.15357+233_15357+234delinsTG XP_011539421.1:n.15357+233_15357+234delinsTG
XM_011541120.1:c.15354+233_15354+234delinsTG XP_011539422.1:n.15354+233_15354+234delinsTG
XM_011541121.1:c.15321+233_15321+234delinsTG XP_011539423.1:n.15321+233_15321+234delinsTG
XM_011541108.3:c.15591+233_15591+234delinsTG XP_011539410.2:n.15591+233_15591+234delinsTG
XM_011541109.3:c.15588+233_15588+234delinsTG XP_011539411.2:n.15588+233_15588+234delinsTG
XM_011541110.3:c.15588+233_15588+234delinsTG XP_011539412.2:n.15588+233_15588+234delinsTG
XM_011541111.3:c.15588+233_15588+234delinsTG XP_011539413.2:n.15588+233_15588+234delinsTG
XM_011541112.3:c.15576+233_15576+234delinsTG XP_011539414.2:n.15576+233_15576+234delinsTG
XM_011541113.3:c.15573+233_15573+234delinsTG XP_011539415.2:n.15573+233_15573+234delinsTG
XM_011541114.3:c.15573+233_15573+234delinsTG XP_011539416.2:n.15573+233_15573+234delinsTG
XM_011541115.3:c.15567+233_15567+234delinsTG XP_011539417.2:n.15567+233_15567+234delinsTG
XM_011541116.3:c.15558+233_15558+234delinsTG XP_011539418.2:n.15558+233_15558+234delinsTG
XM_011541117.3:c.15507+233_15507+234delinsTG XP_011539419.2:n.15507+233_15507+234delinsTG
XM_011541118.3:c.15504+233_15504+234delinsTG XP_011539420.2:n.15504+233_15504+234delinsTG
XM_011541119.3:c.15471+233_15471+234delinsTG XP_011539421.2:n.15471+233_15471+234delinsTG
XM_011541120.3:c.15468+233_15468+234delinsTG XP_011539422.2:n.15468+233_15468+234delinsTG
XM_011541121.3:c.15435+233_15435+234delinsTG XP_011539423.2:n.15435+233_15435+234delinsTG
XM_017000822.2:c.15570+233_15570+234delinsTG XP_016856311.2:n.15570+233_15570+234delinsTG
XM_017000823.2:c.15543+233_15543+234delinsTG XP_016856312.2:n.15543+233_15543+234delinsTG
XM_017000824.2:c.15489+233_15489+234delinsTG XP_016856313.2:n.15489+233_15489+234delinsTG
XM_017000825.2:c.15474+233_15474+234delinsTG XP_016856314.2:n.15474+233_15474+234delinsTG
XM_017000826.2:c.15471+233_15471+234delinsTG XP_016856315.2:n.15471+233_15471+234delinsTG
XM_017000827.2:c.15456+233_15456+234delinsTG XP_016856316.2:n.15456+233_15456+234delinsTG
XM_017000828.2:c.15432+233_15432+234delinsTG XP_016856317.2:n.15432+233_15432+234delinsTG
XM_017000829.2:c.15384+233_15384+234delinsTG XP_016856318.2:n.15384+233_15384+234delinsTG
XM_017000830.2:c.15333+233_15333+234delinsTG XP_016856319.2:n.15333+233_15333+234delinsTG
NM_020765.3:c.15324+233_15324+234delinsTG MANE Select NP_065816.2:n.15324+233_15324+234delinsTG