Canonical Allele Identifier: CA2643751313

Gene: UBR4

Linked Data

• gnomAD v4: 1-19077736-AAAAACCAAACCAAACCAAACCAAAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077747_19077771del , CM000663.2:g.19077747_19077771del	GRCh38
NC_000001.10:g.19404241_19404265del , CM000663.1:g.19404241_19404265del	GRCh37
NC_000001.9:g.19276828_19276852del	NCBI36
NG_027669.1:g.137492_137516del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+215_15324+239del MANE Select	ENSP00000364403.3:n.15324+215_15324+239del
ENST00000375224.1:c.2445+215_2445+239del	ENSP00000364372.1:n.2445+215_2445+239del
ENST00000375225.7:c.549+215_549+239del	ENSP00000364373.3:n.549+215_549+239del
ENST00000375254.7:c.15324+215_15324+239del	ENSP00000364403.3:n.15324+215_15324+239del
ENST00000459947.5:n.3331+215_3331+239del
ENST00000486515.1:n.43+24_43+48del
NM_020765.2:c.15324+215_15324+239del	NP_065816.2:n.15324+215_15324+239del
XM_011541108.1:c.15477+215_15477+239del	XP_011539410.1:n.15477+215_15477+239del
XM_011541109.1:c.15474+215_15474+239del	XP_011539411.1:n.15474+215_15474+239del
XM_011541110.1:c.15474+215_15474+239del	XP_011539412.1:n.15474+215_15474+239del
XM_011541111.1:c.15474+215_15474+239del	XP_011539413.1:n.15474+215_15474+239del
XM_011541112.1:c.15462+215_15462+239del	XP_011539414.1:n.15462+215_15462+239del
XM_011541113.1:c.15459+215_15459+239del	XP_011539415.1:n.15459+215_15459+239del
XM_011541114.1:c.15459+215_15459+239del	XP_011539416.1:n.15459+215_15459+239del
XM_011541115.1:c.15453+215_15453+239del	XP_011539417.1:n.15453+215_15453+239del
XM_011541116.1:c.15444+215_15444+239del	XP_011539418.1:n.15444+215_15444+239del
XM_011541117.1:c.15393+215_15393+239del	XP_011539419.1:n.15393+215_15393+239del
XM_011541118.1:c.15390+215_15390+239del	XP_011539420.1:n.15390+215_15390+239del
XM_011541119.1:c.15357+215_15357+239del	XP_011539421.1:n.15357+215_15357+239del
XM_011541120.1:c.15354+215_15354+239del	XP_011539422.1:n.15354+215_15354+239del
XM_011541121.1:c.15321+215_15321+239del	XP_011539423.1:n.15321+215_15321+239del
XM_011541108.3:c.15591+215_15591+239del	XP_011539410.2:n.15591+215_15591+239del
XM_011541109.3:c.15588+215_15588+239del	XP_011539411.2:n.15588+215_15588+239del
XM_011541110.3:c.15588+215_15588+239del	XP_011539412.2:n.15588+215_15588+239del
XM_011541111.3:c.15588+215_15588+239del	XP_011539413.2:n.15588+215_15588+239del
XM_011541112.3:c.15576+215_15576+239del	XP_011539414.2:n.15576+215_15576+239del
XM_011541113.3:c.15573+215_15573+239del	XP_011539415.2:n.15573+215_15573+239del
XM_011541114.3:c.15573+215_15573+239del	XP_011539416.2:n.15573+215_15573+239del
XM_011541115.3:c.15567+215_15567+239del	XP_011539417.2:n.15567+215_15567+239del
XM_011541116.3:c.15558+215_15558+239del	XP_011539418.2:n.15558+215_15558+239del
XM_011541117.3:c.15507+215_15507+239del	XP_011539419.2:n.15507+215_15507+239del
XM_011541118.3:c.15504+215_15504+239del	XP_011539420.2:n.15504+215_15504+239del
XM_011541119.3:c.15471+215_15471+239del	XP_011539421.2:n.15471+215_15471+239del
XM_011541120.3:c.15468+215_15468+239del	XP_011539422.2:n.15468+215_15468+239del
XM_011541121.3:c.15435+215_15435+239del	XP_011539423.2:n.15435+215_15435+239del
XM_017000822.2:c.15570+215_15570+239del	XP_016856311.2:n.15570+215_15570+239del
XM_017000823.2:c.15543+215_15543+239del	XP_016856312.2:n.15543+215_15543+239del
XM_017000824.2:c.15489+215_15489+239del	XP_016856313.2:n.15489+215_15489+239del
XM_017000825.2:c.15474+215_15474+239del	XP_016856314.2:n.15474+215_15474+239del
XM_017000826.2:c.15471+215_15471+239del	XP_016856315.2:n.15471+215_15471+239del
XM_017000827.2:c.15456+215_15456+239del	XP_016856316.2:n.15456+215_15456+239del
XM_017000828.2:c.15432+215_15432+239del	XP_016856317.2:n.15432+215_15432+239del
XM_017000829.2:c.15384+215_15384+239del	XP_016856318.2:n.15384+215_15384+239del
XM_017000830.2:c.15333+215_15333+239del	XP_016856319.2:n.15333+215_15333+239del
NM_020765.3:c.15324+215_15324+239del MANE Select	NP_065816.2:n.15324+215_15324+239del