Canonical Allele Identifier: CA1156956056

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077957_19077959delinsCCT , CM000663.2:g.19077957_19077959delinsCCT	GRCh38
NC_000001.10:g.19404451_19404453delinsCCT , CM000663.1:g.19404451_19404453delinsCCT	GRCh37
NC_000001.9:g.19277038_19277040delinsCCT	NCBI36
NG_027669.1:g.137294_137296delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+17_15324+19delinsAGG MANE Select	ENSP00000364403.3:n.15324+17_15324+19delinsAGG
ENST00000375224.1:c.2445+17_2445+19delinsAGG	ENSP00000364372.1:n.2445+17_2445+19delinsAGG
ENST00000375225.7:c.549+17_549+19delinsAGG	ENSP00000364373.3:n.549+17_549+19delinsAGG
ENST00000375254.7:c.15324+17_15324+19delinsAGG	ENSP00000364403.3:n.15324+17_15324+19delinsAGG
ENST00000459947.5:n.3331+17_3331+19delinsAGG
NM_020765.2:c.15324+17_15324+19delinsAGG	NP_065816.2:n.15324+17_15324+19delinsAGG
XM_011541108.1:c.15477+17_15477+19delinsAGG	XP_011539410.1:n.15477+17_15477+19delinsAGG
XM_011541109.1:c.15474+17_15474+19delinsAGG	XP_011539411.1:n.15474+17_15474+19delinsAGG
XM_011541110.1:c.15474+17_15474+19delinsAGG	XP_011539412.1:n.15474+17_15474+19delinsAGG
XM_011541111.1:c.15474+17_15474+19delinsAGG	XP_011539413.1:n.15474+17_15474+19delinsAGG
XM_011541112.1:c.15462+17_15462+19delinsAGG	XP_011539414.1:n.15462+17_15462+19delinsAGG
XM_011541113.1:c.15459+17_15459+19delinsAGG	XP_011539415.1:n.15459+17_15459+19delinsAGG
XM_011541114.1:c.15459+17_15459+19delinsAGG	XP_011539416.1:n.15459+17_15459+19delinsAGG
XM_011541115.1:c.15453+17_15453+19delinsAGG	XP_011539417.1:n.15453+17_15453+19delinsAGG
XM_011541116.1:c.15444+17_15444+19delinsAGG	XP_011539418.1:n.15444+17_15444+19delinsAGG
XM_011541117.1:c.15393+17_15393+19delinsAGG	XP_011539419.1:n.15393+17_15393+19delinsAGG
XM_011541118.1:c.15390+17_15390+19delinsAGG	XP_011539420.1:n.15390+17_15390+19delinsAGG
XM_011541119.1:c.15357+17_15357+19delinsAGG	XP_011539421.1:n.15357+17_15357+19delinsAGG
XM_011541120.1:c.15354+17_15354+19delinsAGG	XP_011539422.1:n.15354+17_15354+19delinsAGG
XM_011541121.1:c.15321+17_15321+19delinsAGG	XP_011539423.1:n.15321+17_15321+19delinsAGG
XM_011541108.3:c.15591+17_15591+19delinsAGG	XP_011539410.2:n.15591+17_15591+19delinsAGG
XM_011541109.3:c.15588+17_15588+19delinsAGG	XP_011539411.2:n.15588+17_15588+19delinsAGG
XM_011541110.3:c.15588+17_15588+19delinsAGG	XP_011539412.2:n.15588+17_15588+19delinsAGG
XM_011541111.3:c.15588+17_15588+19delinsAGG	XP_011539413.2:n.15588+17_15588+19delinsAGG
XM_011541112.3:c.15576+17_15576+19delinsAGG	XP_011539414.2:n.15576+17_15576+19delinsAGG
XM_011541113.3:c.15573+17_15573+19delinsAGG	XP_011539415.2:n.15573+17_15573+19delinsAGG
XM_011541114.3:c.15573+17_15573+19delinsAGG	XP_011539416.2:n.15573+17_15573+19delinsAGG
XM_011541115.3:c.15567+17_15567+19delinsAGG	XP_011539417.2:n.15567+17_15567+19delinsAGG
XM_011541116.3:c.15558+17_15558+19delinsAGG	XP_011539418.2:n.15558+17_15558+19delinsAGG
XM_011541117.3:c.15507+17_15507+19delinsAGG	XP_011539419.2:n.15507+17_15507+19delinsAGG
XM_011541118.3:c.15504+17_15504+19delinsAGG	XP_011539420.2:n.15504+17_15504+19delinsAGG
XM_011541119.3:c.15471+17_15471+19delinsAGG	XP_011539421.2:n.15471+17_15471+19delinsAGG
XM_011541120.3:c.15468+17_15468+19delinsAGG	XP_011539422.2:n.15468+17_15468+19delinsAGG
XM_011541121.3:c.15435+17_15435+19delinsAGG	XP_011539423.2:n.15435+17_15435+19delinsAGG
XM_017000822.2:c.15570+17_15570+19delinsAGG	XP_016856311.2:n.15570+17_15570+19delinsAGG
XM_017000823.2:c.15543+17_15543+19delinsAGG	XP_016856312.2:n.15543+17_15543+19delinsAGG
XM_017000824.2:c.15489+17_15489+19delinsAGG	XP_016856313.2:n.15489+17_15489+19delinsAGG
XM_017000825.2:c.15474+17_15474+19delinsAGG	XP_016856314.2:n.15474+17_15474+19delinsAGG
XM_017000826.2:c.15471+17_15471+19delinsAGG	XP_016856315.2:n.15471+17_15471+19delinsAGG
XM_017000827.2:c.15456+17_15456+19delinsAGG	XP_016856316.2:n.15456+17_15456+19delinsAGG
XM_017000828.2:c.15432+17_15432+19delinsAGG	XP_016856317.2:n.15432+17_15432+19delinsAGG
XM_017000829.2:c.15384+17_15384+19delinsAGG	XP_016856318.2:n.15384+17_15384+19delinsAGG
XM_017000830.2:c.15333+17_15333+19delinsAGG	XP_016856319.2:n.15333+17_15333+19delinsAGG
NM_020765.3:c.15324+17_15324+19delinsAGG MANE Select	NP_065816.2:n.15324+17_15324+19delinsAGG