Canonical Allele Identifier: CA2574241770

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077741_19077744del , CM000663.2:g.19077741_19077744del	GRCh38
NC_000001.10:g.19404235_19404238del , CM000663.1:g.19404235_19404238del	GRCh37
NC_000001.9:g.19276822_19276825del	NCBI36
NG_027669.1:g.137511_137514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+234_15324+237del MANE Select	ENSP00000364403.3:n.15324+234_15324+237del
ENST00000375224.1:c.2445+234_2445+237del	ENSP00000364372.1:n.2445+234_2445+237del
ENST00000375225.7:c.549+234_549+237del	ENSP00000364373.3:n.549+234_549+237del
ENST00000375254.7:c.15324+234_15324+237del	ENSP00000364403.3:n.15324+234_15324+237del
ENST00000459947.5:n.3331+234_3331+237del
ENST00000486515.1:n.43+43_43+46del
NM_020765.2:c.15324+234_15324+237del	NP_065816.2:n.15324+234_15324+237del
XM_011541108.1:c.15477+234_15477+237del	XP_011539410.1:n.15477+234_15477+237del
XM_011541109.1:c.15474+234_15474+237del	XP_011539411.1:n.15474+234_15474+237del
XM_011541110.1:c.15474+234_15474+237del	XP_011539412.1:n.15474+234_15474+237del
XM_011541111.1:c.15474+234_15474+237del	XP_011539413.1:n.15474+234_15474+237del
XM_011541112.1:c.15462+234_15462+237del	XP_011539414.1:n.15462+234_15462+237del
XM_011541113.1:c.15459+234_15459+237del	XP_011539415.1:n.15459+234_15459+237del
XM_011541114.1:c.15459+234_15459+237del	XP_011539416.1:n.15459+234_15459+237del
XM_011541115.1:c.15453+234_15453+237del	XP_011539417.1:n.15453+234_15453+237del
XM_011541116.1:c.15444+234_15444+237del	XP_011539418.1:n.15444+234_15444+237del
XM_011541117.1:c.15393+234_15393+237del	XP_011539419.1:n.15393+234_15393+237del
XM_011541118.1:c.15390+234_15390+237del	XP_011539420.1:n.15390+234_15390+237del
XM_011541119.1:c.15357+234_15357+237del	XP_011539421.1:n.15357+234_15357+237del
XM_011541120.1:c.15354+234_15354+237del	XP_011539422.1:n.15354+234_15354+237del
XM_011541121.1:c.15321+234_15321+237del	XP_011539423.1:n.15321+234_15321+237del
XM_011541108.3:c.15591+234_15591+237del	XP_011539410.2:n.15591+234_15591+237del
XM_011541109.3:c.15588+234_15588+237del	XP_011539411.2:n.15588+234_15588+237del
XM_011541110.3:c.15588+234_15588+237del	XP_011539412.2:n.15588+234_15588+237del
XM_011541111.3:c.15588+234_15588+237del	XP_011539413.2:n.15588+234_15588+237del
XM_011541112.3:c.15576+234_15576+237del	XP_011539414.2:n.15576+234_15576+237del
XM_011541113.3:c.15573+234_15573+237del	XP_011539415.2:n.15573+234_15573+237del
XM_011541114.3:c.15573+234_15573+237del	XP_011539416.2:n.15573+234_15573+237del
XM_011541115.3:c.15567+234_15567+237del	XP_011539417.2:n.15567+234_15567+237del
XM_011541116.3:c.15558+234_15558+237del	XP_011539418.2:n.15558+234_15558+237del
XM_011541117.3:c.15507+234_15507+237del	XP_011539419.2:n.15507+234_15507+237del
XM_011541118.3:c.15504+234_15504+237del	XP_011539420.2:n.15504+234_15504+237del
XM_011541119.3:c.15471+234_15471+237del	XP_011539421.2:n.15471+234_15471+237del
XM_011541120.3:c.15468+234_15468+237del	XP_011539422.2:n.15468+234_15468+237del
XM_011541121.3:c.15435+234_15435+237del	XP_011539423.2:n.15435+234_15435+237del
XM_017000822.2:c.15570+234_15570+237del	XP_016856311.2:n.15570+234_15570+237del
XM_017000823.2:c.15543+234_15543+237del	XP_016856312.2:n.15543+234_15543+237del
XM_017000824.2:c.15489+234_15489+237del	XP_016856313.2:n.15489+234_15489+237del
XM_017000825.2:c.15474+234_15474+237del	XP_016856314.2:n.15474+234_15474+237del
XM_017000826.2:c.15471+234_15471+237del	XP_016856315.2:n.15471+234_15471+237del
XM_017000827.2:c.15456+234_15456+237del	XP_016856316.2:n.15456+234_15456+237del
XM_017000828.2:c.15432+234_15432+237del	XP_016856317.2:n.15432+234_15432+237del
XM_017000829.2:c.15384+234_15384+237del	XP_016856318.2:n.15384+234_15384+237del
XM_017000830.2:c.15333+234_15333+237del	XP_016856319.2:n.15333+234_15333+237del
NM_020765.3:c.15324+234_15324+237del MANE Select	NP_065816.2:n.15324+234_15324+237del