Canonical Allele Identifier: CA1156955969

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077762_19077767delinsAAAACC , CM000663.2:g.19077762_19077767delinsAAAACC	GRCh38
NC_000001.10:g.19404256_19404261delinsAAAACC , CM000663.1:g.19404256_19404261delinsAAAACC	GRCh37
NC_000001.9:g.19276843_19276848delinsAAAACC	NCBI36
NG_027669.1:g.137486_137491delinsGGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+209_15324+214delinsGGTTTT MANE Select	ENSP00000364403.3:n.15324+209_15324+214delinsGGTTTT
ENST00000375224.1:c.2445+209_2445+214delinsGGTTTT	ENSP00000364372.1:n.2445+209_2445+214delinsGGTTTT
ENST00000375225.7:c.549+209_549+214delinsGGTTTT	ENSP00000364373.3:n.549+209_549+214delinsGGTTTT
ENST00000375254.7:c.15324+209_15324+214delinsGGTTTT	ENSP00000364403.3:n.15324+209_15324+214delinsGGTTTT
ENST00000459947.5:n.3331+209_3331+214delinsGGTTTT
ENST00000486515.1:n.43+18_43+23delinsGGTTTT
NM_020765.2:c.15324+209_15324+214delinsGGTTTT	NP_065816.2:n.15324+209_15324+214delinsGGTTTT
XM_011541108.1:c.15477+209_15477+214delinsGGTTTT	XP_011539410.1:n.15477+209_15477+214delinsGGTTTT
XM_011541109.1:c.15474+209_15474+214delinsGGTTTT	XP_011539411.1:n.15474+209_15474+214delinsGGTTTT
XM_011541110.1:c.15474+209_15474+214delinsGGTTTT	XP_011539412.1:n.15474+209_15474+214delinsGGTTTT
XM_011541111.1:c.15474+209_15474+214delinsGGTTTT	XP_011539413.1:n.15474+209_15474+214delinsGGTTTT
XM_011541112.1:c.15462+209_15462+214delinsGGTTTT	XP_011539414.1:n.15462+209_15462+214delinsGGTTTT
XM_011541113.1:c.15459+209_15459+214delinsGGTTTT	XP_011539415.1:n.15459+209_15459+214delinsGGTTTT
XM_011541114.1:c.15459+209_15459+214delinsGGTTTT	XP_011539416.1:n.15459+209_15459+214delinsGGTTTT
XM_011541115.1:c.15453+209_15453+214delinsGGTTTT	XP_011539417.1:n.15453+209_15453+214delinsGGTTTT
XM_011541116.1:c.15444+209_15444+214delinsGGTTTT	XP_011539418.1:n.15444+209_15444+214delinsGGTTTT
XM_011541117.1:c.15393+209_15393+214delinsGGTTTT	XP_011539419.1:n.15393+209_15393+214delinsGGTTTT
XM_011541118.1:c.15390+209_15390+214delinsGGTTTT	XP_011539420.1:n.15390+209_15390+214delinsGGTTTT
XM_011541119.1:c.15357+209_15357+214delinsGGTTTT	XP_011539421.1:n.15357+209_15357+214delinsGGTTTT
XM_011541120.1:c.15354+209_15354+214delinsGGTTTT	XP_011539422.1:n.15354+209_15354+214delinsGGTTTT
XM_011541121.1:c.15321+209_15321+214delinsGGTTTT	XP_011539423.1:n.15321+209_15321+214delinsGGTTTT
XM_011541108.3:c.15591+209_15591+214delinsGGTTTT	XP_011539410.2:n.15591+209_15591+214delinsGGTTTT
XM_011541109.3:c.15588+209_15588+214delinsGGTTTT	XP_011539411.2:n.15588+209_15588+214delinsGGTTTT
XM_011541110.3:c.15588+209_15588+214delinsGGTTTT	XP_011539412.2:n.15588+209_15588+214delinsGGTTTT
XM_011541111.3:c.15588+209_15588+214delinsGGTTTT	XP_011539413.2:n.15588+209_15588+214delinsGGTTTT
XM_011541112.3:c.15576+209_15576+214delinsGGTTTT	XP_011539414.2:n.15576+209_15576+214delinsGGTTTT
XM_011541113.3:c.15573+209_15573+214delinsGGTTTT	XP_011539415.2:n.15573+209_15573+214delinsGGTTTT
XM_011541114.3:c.15573+209_15573+214delinsGGTTTT	XP_011539416.2:n.15573+209_15573+214delinsGGTTTT
XM_011541115.3:c.15567+209_15567+214delinsGGTTTT	XP_011539417.2:n.15567+209_15567+214delinsGGTTTT
XM_011541116.3:c.15558+209_15558+214delinsGGTTTT	XP_011539418.2:n.15558+209_15558+214delinsGGTTTT
XM_011541117.3:c.15507+209_15507+214delinsGGTTTT	XP_011539419.2:n.15507+209_15507+214delinsGGTTTT
XM_011541118.3:c.15504+209_15504+214delinsGGTTTT	XP_011539420.2:n.15504+209_15504+214delinsGGTTTT
XM_011541119.3:c.15471+209_15471+214delinsGGTTTT	XP_011539421.2:n.15471+209_15471+214delinsGGTTTT
XM_011541120.3:c.15468+209_15468+214delinsGGTTTT	XP_011539422.2:n.15468+209_15468+214delinsGGTTTT
XM_011541121.3:c.15435+209_15435+214delinsGGTTTT	XP_011539423.2:n.15435+209_15435+214delinsGGTTTT
XM_017000822.2:c.15570+209_15570+214delinsGGTTTT	XP_016856311.2:n.15570+209_15570+214delinsGGTTTT
XM_017000823.2:c.15543+209_15543+214delinsGGTTTT	XP_016856312.2:n.15543+209_15543+214delinsGGTTTT
XM_017000824.2:c.15489+209_15489+214delinsGGTTTT	XP_016856313.2:n.15489+209_15489+214delinsGGTTTT
XM_017000825.2:c.15474+209_15474+214delinsGGTTTT	XP_016856314.2:n.15474+209_15474+214delinsGGTTTT
XM_017000826.2:c.15471+209_15471+214delinsGGTTTT	XP_016856315.2:n.15471+209_15471+214delinsGGTTTT
XM_017000827.2:c.15456+209_15456+214delinsGGTTTT	XP_016856316.2:n.15456+209_15456+214delinsGGTTTT
XM_017000828.2:c.15432+209_15432+214delinsGGTTTT	XP_016856317.2:n.15432+209_15432+214delinsGGTTTT
XM_017000829.2:c.15384+209_15384+214delinsGGTTTT	XP_016856318.2:n.15384+209_15384+214delinsGGTTTT
XM_017000830.2:c.15333+209_15333+214delinsGGTTTT	XP_016856319.2:n.15333+209_15333+214delinsGGTTTT
NM_020765.3:c.15324+209_15324+214delinsGGTTTT MANE Select	NP_065816.2:n.15324+209_15324+214delinsGGTTTT