Canonical Allele Identifier: CA1156956017

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077875_19077878delinsCGGA , CM000663.2:g.19077875_19077878delinsCGGA	GRCh38
NC_000001.10:g.19404369_19404372delinsCGGA , CM000663.1:g.19404369_19404372delinsCGGA	GRCh37
NC_000001.9:g.19276956_19276959delinsCGGA	NCBI36
NG_027669.1:g.137375_137378delinsTCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+98_15324+101delinsTCCG MANE Select	ENSP00000364403.3:n.15324+98_15324+101delinsTCCG
ENST00000375224.1:c.2445+98_2445+101delinsTCCG	ENSP00000364372.1:n.2445+98_2445+101delinsTCCG
ENST00000375225.7:c.549+98_549+101delinsTCCG	ENSP00000364373.3:n.549+98_549+101delinsTCCG
ENST00000375254.7:c.15324+98_15324+101delinsTCCG	ENSP00000364403.3:n.15324+98_15324+101delinsTCCG
ENST00000459947.5:n.3331+98_3331+101delinsTCCG
NM_020765.2:c.15324+98_15324+101delinsTCCG	NP_065816.2:n.15324+98_15324+101delinsTCCG
XM_011541108.1:c.15477+98_15477+101delinsTCCG	XP_011539410.1:n.15477+98_15477+101delinsTCCG
XM_011541109.1:c.15474+98_15474+101delinsTCCG	XP_011539411.1:n.15474+98_15474+101delinsTCCG
XM_011541110.1:c.15474+98_15474+101delinsTCCG	XP_011539412.1:n.15474+98_15474+101delinsTCCG
XM_011541111.1:c.15474+98_15474+101delinsTCCG	XP_011539413.1:n.15474+98_15474+101delinsTCCG
XM_011541112.1:c.15462+98_15462+101delinsTCCG	XP_011539414.1:n.15462+98_15462+101delinsTCCG
XM_011541113.1:c.15459+98_15459+101delinsTCCG	XP_011539415.1:n.15459+98_15459+101delinsTCCG
XM_011541114.1:c.15459+98_15459+101delinsTCCG	XP_011539416.1:n.15459+98_15459+101delinsTCCG
XM_011541115.1:c.15453+98_15453+101delinsTCCG	XP_011539417.1:n.15453+98_15453+101delinsTCCG
XM_011541116.1:c.15444+98_15444+101delinsTCCG	XP_011539418.1:n.15444+98_15444+101delinsTCCG
XM_011541117.1:c.15393+98_15393+101delinsTCCG	XP_011539419.1:n.15393+98_15393+101delinsTCCG
XM_011541118.1:c.15390+98_15390+101delinsTCCG	XP_011539420.1:n.15390+98_15390+101delinsTCCG
XM_011541119.1:c.15357+98_15357+101delinsTCCG	XP_011539421.1:n.15357+98_15357+101delinsTCCG
XM_011541120.1:c.15354+98_15354+101delinsTCCG	XP_011539422.1:n.15354+98_15354+101delinsTCCG
XM_011541121.1:c.15321+98_15321+101delinsTCCG	XP_011539423.1:n.15321+98_15321+101delinsTCCG
XM_011541108.3:c.15591+98_15591+101delinsTCCG	XP_011539410.2:n.15591+98_15591+101delinsTCCG
XM_011541109.3:c.15588+98_15588+101delinsTCCG	XP_011539411.2:n.15588+98_15588+101delinsTCCG
XM_011541110.3:c.15588+98_15588+101delinsTCCG	XP_011539412.2:n.15588+98_15588+101delinsTCCG
XM_011541111.3:c.15588+98_15588+101delinsTCCG	XP_011539413.2:n.15588+98_15588+101delinsTCCG
XM_011541112.3:c.15576+98_15576+101delinsTCCG	XP_011539414.2:n.15576+98_15576+101delinsTCCG
XM_011541113.3:c.15573+98_15573+101delinsTCCG	XP_011539415.2:n.15573+98_15573+101delinsTCCG
XM_011541114.3:c.15573+98_15573+101delinsTCCG	XP_011539416.2:n.15573+98_15573+101delinsTCCG
XM_011541115.3:c.15567+98_15567+101delinsTCCG	XP_011539417.2:n.15567+98_15567+101delinsTCCG
XM_011541116.3:c.15558+98_15558+101delinsTCCG	XP_011539418.2:n.15558+98_15558+101delinsTCCG
XM_011541117.3:c.15507+98_15507+101delinsTCCG	XP_011539419.2:n.15507+98_15507+101delinsTCCG
XM_011541118.3:c.15504+98_15504+101delinsTCCG	XP_011539420.2:n.15504+98_15504+101delinsTCCG
XM_011541119.3:c.15471+98_15471+101delinsTCCG	XP_011539421.2:n.15471+98_15471+101delinsTCCG
XM_011541120.3:c.15468+98_15468+101delinsTCCG	XP_011539422.2:n.15468+98_15468+101delinsTCCG
XM_011541121.3:c.15435+98_15435+101delinsTCCG	XP_011539423.2:n.15435+98_15435+101delinsTCCG
XM_017000822.2:c.15570+98_15570+101delinsTCCG	XP_016856311.2:n.15570+98_15570+101delinsTCCG
XM_017000823.2:c.15543+98_15543+101delinsTCCG	XP_016856312.2:n.15543+98_15543+101delinsTCCG
XM_017000824.2:c.15489+98_15489+101delinsTCCG	XP_016856313.2:n.15489+98_15489+101delinsTCCG
XM_017000825.2:c.15474+98_15474+101delinsTCCG	XP_016856314.2:n.15474+98_15474+101delinsTCCG
XM_017000826.2:c.15471+98_15471+101delinsTCCG	XP_016856315.2:n.15471+98_15471+101delinsTCCG
XM_017000827.2:c.15456+98_15456+101delinsTCCG	XP_016856316.2:n.15456+98_15456+101delinsTCCG
XM_017000828.2:c.15432+98_15432+101delinsTCCG	XP_016856317.2:n.15432+98_15432+101delinsTCCG
XM_017000829.2:c.15384+98_15384+101delinsTCCG	XP_016856318.2:n.15384+98_15384+101delinsTCCG
XM_017000830.2:c.15333+98_15333+101delinsTCCG	XP_016856319.2:n.15333+98_15333+101delinsTCCG
NM_020765.3:c.15324+98_15324+101delinsTCCG MANE Select	NP_065816.2:n.15324+98_15324+101delinsTCCG