Canonical Allele Identifier: CA1156956025

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077888_19077889delinsAT , CM000663.2:g.19077888_19077889delinsAT	GRCh38
NC_000001.10:g.19404382_19404383delinsAT , CM000663.1:g.19404382_19404383delinsAT	GRCh37
NC_000001.9:g.19276969_19276970delinsAT	NCBI36
NG_027669.1:g.137364_137365delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+87_15324+88delinsAT MANE Select	ENSP00000364403.3:n.15324+87_15324+88delinsAT
ENST00000375224.1:c.2445+87_2445+88delinsAT	ENSP00000364372.1:n.2445+87_2445+88delinsAT
ENST00000375225.7:c.549+87_549+88delinsAT	ENSP00000364373.3:n.549+87_549+88delinsAT
ENST00000375254.7:c.15324+87_15324+88delinsAT	ENSP00000364403.3:n.15324+87_15324+88delinsAT
ENST00000459947.5:n.3331+87_3331+88delinsAT
NM_020765.2:c.15324+87_15324+88delinsAT	NP_065816.2:n.15324+87_15324+88delinsAT
XM_011541108.1:c.15477+87_15477+88delinsAT	XP_011539410.1:n.15477+87_15477+88delinsAT
XM_011541109.1:c.15474+87_15474+88delinsAT	XP_011539411.1:n.15474+87_15474+88delinsAT
XM_011541110.1:c.15474+87_15474+88delinsAT	XP_011539412.1:n.15474+87_15474+88delinsAT
XM_011541111.1:c.15474+87_15474+88delinsAT	XP_011539413.1:n.15474+87_15474+88delinsAT
XM_011541112.1:c.15462+87_15462+88delinsAT	XP_011539414.1:n.15462+87_15462+88delinsAT
XM_011541113.1:c.15459+87_15459+88delinsAT	XP_011539415.1:n.15459+87_15459+88delinsAT
XM_011541114.1:c.15459+87_15459+88delinsAT	XP_011539416.1:n.15459+87_15459+88delinsAT
XM_011541115.1:c.15453+87_15453+88delinsAT	XP_011539417.1:n.15453+87_15453+88delinsAT
XM_011541116.1:c.15444+87_15444+88delinsAT	XP_011539418.1:n.15444+87_15444+88delinsAT
XM_011541117.1:c.15393+87_15393+88delinsAT	XP_011539419.1:n.15393+87_15393+88delinsAT
XM_011541118.1:c.15390+87_15390+88delinsAT	XP_011539420.1:n.15390+87_15390+88delinsAT
XM_011541119.1:c.15357+87_15357+88delinsAT	XP_011539421.1:n.15357+87_15357+88delinsAT
XM_011541120.1:c.15354+87_15354+88delinsAT	XP_011539422.1:n.15354+87_15354+88delinsAT
XM_011541121.1:c.15321+87_15321+88delinsAT	XP_011539423.1:n.15321+87_15321+88delinsAT
XM_011541108.3:c.15591+87_15591+88delinsAT	XP_011539410.2:n.15591+87_15591+88delinsAT
XM_011541109.3:c.15588+87_15588+88delinsAT	XP_011539411.2:n.15588+87_15588+88delinsAT
XM_011541110.3:c.15588+87_15588+88delinsAT	XP_011539412.2:n.15588+87_15588+88delinsAT
XM_011541111.3:c.15588+87_15588+88delinsAT	XP_011539413.2:n.15588+87_15588+88delinsAT
XM_011541112.3:c.15576+87_15576+88delinsAT	XP_011539414.2:n.15576+87_15576+88delinsAT
XM_011541113.3:c.15573+87_15573+88delinsAT	XP_011539415.2:n.15573+87_15573+88delinsAT
XM_011541114.3:c.15573+87_15573+88delinsAT	XP_011539416.2:n.15573+87_15573+88delinsAT
XM_011541115.3:c.15567+87_15567+88delinsAT	XP_011539417.2:n.15567+87_15567+88delinsAT
XM_011541116.3:c.15558+87_15558+88delinsAT	XP_011539418.2:n.15558+87_15558+88delinsAT
XM_011541117.3:c.15507+87_15507+88delinsAT	XP_011539419.2:n.15507+87_15507+88delinsAT
XM_011541118.3:c.15504+87_15504+88delinsAT	XP_011539420.2:n.15504+87_15504+88delinsAT
XM_011541119.3:c.15471+87_15471+88delinsAT	XP_011539421.2:n.15471+87_15471+88delinsAT
XM_011541120.3:c.15468+87_15468+88delinsAT	XP_011539422.2:n.15468+87_15468+88delinsAT
XM_011541121.3:c.15435+87_15435+88delinsAT	XP_011539423.2:n.15435+87_15435+88delinsAT
XM_017000822.2:c.15570+87_15570+88delinsAT	XP_016856311.2:n.15570+87_15570+88delinsAT
XM_017000823.2:c.15543+87_15543+88delinsAT	XP_016856312.2:n.15543+87_15543+88delinsAT
XM_017000824.2:c.15489+87_15489+88delinsAT	XP_016856313.2:n.15489+87_15489+88delinsAT
XM_017000825.2:c.15474+87_15474+88delinsAT	XP_016856314.2:n.15474+87_15474+88delinsAT
XM_017000826.2:c.15471+87_15471+88delinsAT	XP_016856315.2:n.15471+87_15471+88delinsAT
XM_017000827.2:c.15456+87_15456+88delinsAT	XP_016856316.2:n.15456+87_15456+88delinsAT
XM_017000828.2:c.15432+87_15432+88delinsAT	XP_016856317.2:n.15432+87_15432+88delinsAT
XM_017000829.2:c.15384+87_15384+88delinsAT	XP_016856318.2:n.15384+87_15384+88delinsAT
XM_017000830.2:c.15333+87_15333+88delinsAT	XP_016856319.2:n.15333+87_15333+88delinsAT
NM_020765.3:c.15324+87_15324+88delinsAT MANE Select	NP_065816.2:n.15324+87_15324+88delinsAT