Canonical Allele Identifier: CA1156955967

Gene: UBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077757_19077762delinsCAAACA , CM000663.2:g.19077757_19077762delinsCAAACA	GRCh38
NC_000001.10:g.19404251_19404256delinsCAAACA , CM000663.1:g.19404251_19404256delinsCAAACA	GRCh37
NC_000001.9:g.19276838_19276843delinsCAAACA	NCBI36
NG_027669.1:g.137491_137496delinsTGTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+214_15324+219delinsTGTTTG MANE Select	ENSP00000364403.3:n.15324+214_15324+219delinsTGTTTG
ENST00000375224.1:c.2445+214_2445+219delinsTGTTTG	ENSP00000364372.1:n.2445+214_2445+219delinsTGTTTG
ENST00000375225.7:c.549+214_549+219delinsTGTTTG	ENSP00000364373.3:n.549+214_549+219delinsTGTTTG
ENST00000375254.7:c.15324+214_15324+219delinsTGTTTG	ENSP00000364403.3:n.15324+214_15324+219delinsTGTTTG
ENST00000459947.5:n.3331+214_3331+219delinsTGTTTG
ENST00000486515.1:n.43+23_43+28delinsTGTTTG
NM_020765.2:c.15324+214_15324+219delinsTGTTTG	NP_065816.2:n.15324+214_15324+219delinsTGTTTG
XM_011541108.1:c.15477+214_15477+219delinsTGTTTG	XP_011539410.1:n.15477+214_15477+219delinsTGTTTG
XM_011541109.1:c.15474+214_15474+219delinsTGTTTG	XP_011539411.1:n.15474+214_15474+219delinsTGTTTG
XM_011541110.1:c.15474+214_15474+219delinsTGTTTG	XP_011539412.1:n.15474+214_15474+219delinsTGTTTG
XM_011541111.1:c.15474+214_15474+219delinsTGTTTG	XP_011539413.1:n.15474+214_15474+219delinsTGTTTG
XM_011541112.1:c.15462+214_15462+219delinsTGTTTG	XP_011539414.1:n.15462+214_15462+219delinsTGTTTG
XM_011541113.1:c.15459+214_15459+219delinsTGTTTG	XP_011539415.1:n.15459+214_15459+219delinsTGTTTG
XM_011541114.1:c.15459+214_15459+219delinsTGTTTG	XP_011539416.1:n.15459+214_15459+219delinsTGTTTG
XM_011541115.1:c.15453+214_15453+219delinsTGTTTG	XP_011539417.1:n.15453+214_15453+219delinsTGTTTG
XM_011541116.1:c.15444+214_15444+219delinsTGTTTG	XP_011539418.1:n.15444+214_15444+219delinsTGTTTG
XM_011541117.1:c.15393+214_15393+219delinsTGTTTG	XP_011539419.1:n.15393+214_15393+219delinsTGTTTG
XM_011541118.1:c.15390+214_15390+219delinsTGTTTG	XP_011539420.1:n.15390+214_15390+219delinsTGTTTG
XM_011541119.1:c.15357+214_15357+219delinsTGTTTG	XP_011539421.1:n.15357+214_15357+219delinsTGTTTG
XM_011541120.1:c.15354+214_15354+219delinsTGTTTG	XP_011539422.1:n.15354+214_15354+219delinsTGTTTG
XM_011541121.1:c.15321+214_15321+219delinsTGTTTG	XP_011539423.1:n.15321+214_15321+219delinsTGTTTG
XM_011541108.3:c.15591+214_15591+219delinsTGTTTG	XP_011539410.2:n.15591+214_15591+219delinsTGTTTG
XM_011541109.3:c.15588+214_15588+219delinsTGTTTG	XP_011539411.2:n.15588+214_15588+219delinsTGTTTG
XM_011541110.3:c.15588+214_15588+219delinsTGTTTG	XP_011539412.2:n.15588+214_15588+219delinsTGTTTG
XM_011541111.3:c.15588+214_15588+219delinsTGTTTG	XP_011539413.2:n.15588+214_15588+219delinsTGTTTG
XM_011541112.3:c.15576+214_15576+219delinsTGTTTG	XP_011539414.2:n.15576+214_15576+219delinsTGTTTG
XM_011541113.3:c.15573+214_15573+219delinsTGTTTG	XP_011539415.2:n.15573+214_15573+219delinsTGTTTG
XM_011541114.3:c.15573+214_15573+219delinsTGTTTG	XP_011539416.2:n.15573+214_15573+219delinsTGTTTG
XM_011541115.3:c.15567+214_15567+219delinsTGTTTG	XP_011539417.2:n.15567+214_15567+219delinsTGTTTG
XM_011541116.3:c.15558+214_15558+219delinsTGTTTG	XP_011539418.2:n.15558+214_15558+219delinsTGTTTG
XM_011541117.3:c.15507+214_15507+219delinsTGTTTG	XP_011539419.2:n.15507+214_15507+219delinsTGTTTG
XM_011541118.3:c.15504+214_15504+219delinsTGTTTG	XP_011539420.2:n.15504+214_15504+219delinsTGTTTG
XM_011541119.3:c.15471+214_15471+219delinsTGTTTG	XP_011539421.2:n.15471+214_15471+219delinsTGTTTG
XM_011541120.3:c.15468+214_15468+219delinsTGTTTG	XP_011539422.2:n.15468+214_15468+219delinsTGTTTG
XM_011541121.3:c.15435+214_15435+219delinsTGTTTG	XP_011539423.2:n.15435+214_15435+219delinsTGTTTG
XM_017000822.2:c.15570+214_15570+219delinsTGTTTG	XP_016856311.2:n.15570+214_15570+219delinsTGTTTG
XM_017000823.2:c.15543+214_15543+219delinsTGTTTG	XP_016856312.2:n.15543+214_15543+219delinsTGTTTG
XM_017000824.2:c.15489+214_15489+219delinsTGTTTG	XP_016856313.2:n.15489+214_15489+219delinsTGTTTG
XM_017000825.2:c.15474+214_15474+219delinsTGTTTG	XP_016856314.2:n.15474+214_15474+219delinsTGTTTG
XM_017000826.2:c.15471+214_15471+219delinsTGTTTG	XP_016856315.2:n.15471+214_15471+219delinsTGTTTG
XM_017000827.2:c.15456+214_15456+219delinsTGTTTG	XP_016856316.2:n.15456+214_15456+219delinsTGTTTG
XM_017000828.2:c.15432+214_15432+219delinsTGTTTG	XP_016856317.2:n.15432+214_15432+219delinsTGTTTG
XM_017000829.2:c.15384+214_15384+219delinsTGTTTG	XP_016856318.2:n.15384+214_15384+219delinsTGTTTG
XM_017000830.2:c.15333+214_15333+219delinsTGTTTG	XP_016856319.2:n.15333+214_15333+219delinsTGTTTG
NM_020765.3:c.15324+214_15324+219delinsTGTTTG MANE Select	NP_065816.2:n.15324+214_15324+219delinsTGTTTG