Canonical Allele Identifier: CA2643751265

Gene: UBR4

Linked Data

• gnomAD v4: 1-19077690-G-GCACT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077691_19077692insACTC , CM000663.2:g.19077691_19077692insACTC	GRCh38
NC_000001.10:g.19404185_19404186insACTC , CM000663.1:g.19404185_19404186insACTC	GRCh37
NC_000001.9:g.19276772_19276773insACTC	NCBI36
NG_027669.1:g.137562_137563insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+285_15324+286insAGTG MANE Select	ENSP00000364403.3:n.15324+285_15324+286insAGTG
ENST00000375224.1:c.2445+285_2445+286insAGTG	ENSP00000364372.1:n.2445+285_2445+286insAGTG
ENST00000375225.7:c.549+285_549+286insAGTG	ENSP00000364373.3:n.549+285_549+286insAGTG
ENST00000375254.7:c.15324+285_15324+286insAGTG	ENSP00000364403.3:n.15324+285_15324+286insAGTG
ENST00000459947.5:n.3331+285_3331+286insAGTG
ENST00000486515.1:n.43+94_43+95insAGTG
NM_020765.2:c.15324+285_15324+286insAGTG	NP_065816.2:n.15324+285_15324+286insAGTG
XM_011541108.1:c.15477+285_15477+286insAGTG	XP_011539410.1:n.15477+285_15477+286insAGTG
XM_011541109.1:c.15474+285_15474+286insAGTG	XP_011539411.1:n.15474+285_15474+286insAGTG
XM_011541110.1:c.15474+285_15474+286insAGTG	XP_011539412.1:n.15474+285_15474+286insAGTG
XM_011541111.1:c.15474+285_15474+286insAGTG	XP_011539413.1:n.15474+285_15474+286insAGTG
XM_011541112.1:c.15462+285_15462+286insAGTG	XP_011539414.1:n.15462+285_15462+286insAGTG
XM_011541113.1:c.15459+285_15459+286insAGTG	XP_011539415.1:n.15459+285_15459+286insAGTG
XM_011541114.1:c.15459+285_15459+286insAGTG	XP_011539416.1:n.15459+285_15459+286insAGTG
XM_011541115.1:c.15453+285_15453+286insAGTG	XP_011539417.1:n.15453+285_15453+286insAGTG
XM_011541116.1:c.15444+285_15444+286insAGTG	XP_011539418.1:n.15444+285_15444+286insAGTG
XM_011541117.1:c.15393+285_15393+286insAGTG	XP_011539419.1:n.15393+285_15393+286insAGTG
XM_011541118.1:c.15390+285_15390+286insAGTG	XP_011539420.1:n.15390+285_15390+286insAGTG
XM_011541119.1:c.15357+285_15357+286insAGTG	XP_011539421.1:n.15357+285_15357+286insAGTG
XM_011541120.1:c.15354+285_15354+286insAGTG	XP_011539422.1:n.15354+285_15354+286insAGTG
XM_011541121.1:c.15321+285_15321+286insAGTG	XP_011539423.1:n.15321+285_15321+286insAGTG
XM_011541108.3:c.15591+285_15591+286insAGTG	XP_011539410.2:n.15591+285_15591+286insAGTG
XM_011541109.3:c.15588+285_15588+286insAGTG	XP_011539411.2:n.15588+285_15588+286insAGTG
XM_011541110.3:c.15588+285_15588+286insAGTG	XP_011539412.2:n.15588+285_15588+286insAGTG
XM_011541111.3:c.15588+285_15588+286insAGTG	XP_011539413.2:n.15588+285_15588+286insAGTG
XM_011541112.3:c.15576+285_15576+286insAGTG	XP_011539414.2:n.15576+285_15576+286insAGTG
XM_011541113.3:c.15573+285_15573+286insAGTG	XP_011539415.2:n.15573+285_15573+286insAGTG
XM_011541114.3:c.15573+285_15573+286insAGTG	XP_011539416.2:n.15573+285_15573+286insAGTG
XM_011541115.3:c.15567+285_15567+286insAGTG	XP_011539417.2:n.15567+285_15567+286insAGTG
XM_011541116.3:c.15558+285_15558+286insAGTG	XP_011539418.2:n.15558+285_15558+286insAGTG
XM_011541117.3:c.15507+285_15507+286insAGTG	XP_011539419.2:n.15507+285_15507+286insAGTG
XM_011541118.3:c.15504+285_15504+286insAGTG	XP_011539420.2:n.15504+285_15504+286insAGTG
XM_011541119.3:c.15471+285_15471+286insAGTG	XP_011539421.2:n.15471+285_15471+286insAGTG
XM_011541120.3:c.15468+285_15468+286insAGTG	XP_011539422.2:n.15468+285_15468+286insAGTG
XM_011541121.3:c.15435+285_15435+286insAGTG	XP_011539423.2:n.15435+285_15435+286insAGTG
XM_017000822.2:c.15570+285_15570+286insAGTG	XP_016856311.2:n.15570+285_15570+286insAGTG
XM_017000823.2:c.15543+285_15543+286insAGTG	XP_016856312.2:n.15543+285_15543+286insAGTG
XM_017000824.2:c.15489+285_15489+286insAGTG	XP_016856313.2:n.15489+285_15489+286insAGTG
XM_017000825.2:c.15474+285_15474+286insAGTG	XP_016856314.2:n.15474+285_15474+286insAGTG
XM_017000826.2:c.15471+285_15471+286insAGTG	XP_016856315.2:n.15471+285_15471+286insAGTG
XM_017000827.2:c.15456+285_15456+286insAGTG	XP_016856316.2:n.15456+285_15456+286insAGTG
XM_017000828.2:c.15432+285_15432+286insAGTG	XP_016856317.2:n.15432+285_15432+286insAGTG
XM_017000829.2:c.15384+285_15384+286insAGTG	XP_016856318.2:n.15384+285_15384+286insAGTG
XM_017000830.2:c.15333+285_15333+286insAGTG	XP_016856319.2:n.15333+285_15333+286insAGTG
NM_020765.3:c.15324+285_15324+286insAGTG MANE Select	NP_065816.2:n.15324+285_15324+286insAGTG