Canonical Allele Identifier: CA647865

Gene: UBR4

Linked Data

• dbSNP Id: rs553369721
• ExAC: 1:19404231 A / AAAACC
• gnomAD v2: 1-19404231-A-AAAACC
• gnomAD v3: 1-19077737-A-AAAACC
• gnomAD v4: 1-19077737-A-AAAACC
• MyVariant Identifiers: chr1:g.19404241_19404242insAAACC (hg19) ; chr1:g.19404231_19404232insAAACC (hg19) ; chr1:g.19077747_19077748insAAACC (hg38) ; chr1:g.19077737_19077738insAAACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077757_19077761dup , CM000663.2:g.19077757_19077761dup	GRCh38
NC_000001.10:g.19404251_19404255dup , CM000663.1:g.19404251_19404255dup	GRCh37
NC_000001.9:g.19276838_19276842dup	NCBI36
NG_027669.1:g.137511_137515dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+234_15324+238dup MANE Select	ENSP00000364403.3:n.15324+234_15324+238dup
ENST00000375224.1:c.2445+234_2445+238dup	ENSP00000364372.1:n.2445+234_2445+238dup
ENST00000375225.7:c.549+234_549+238dup	ENSP00000364373.3:n.549+234_549+238dup
ENST00000375254.7:c.15324+234_15324+238dup	ENSP00000364403.3:n.15324+234_15324+238dup
ENST00000459947.5:n.3331+234_3331+238dup
ENST00000486515.1:n.43+43_43+47dup
NM_020765.2:c.15324+234_15324+238dup	NP_065816.2:n.15324+234_15324+238dup
XM_011541108.1:c.15477+234_15477+238dup	XP_011539410.1:n.15477+234_15477+238dup
XM_011541109.1:c.15474+234_15474+238dup	XP_011539411.1:n.15474+234_15474+238dup
XM_011541110.1:c.15474+234_15474+238dup	XP_011539412.1:n.15474+234_15474+238dup
XM_011541111.1:c.15474+234_15474+238dup	XP_011539413.1:n.15474+234_15474+238dup
XM_011541112.1:c.15462+234_15462+238dup	XP_011539414.1:n.15462+234_15462+238dup
XM_011541113.1:c.15459+234_15459+238dup	XP_011539415.1:n.15459+234_15459+238dup
XM_011541114.1:c.15459+234_15459+238dup	XP_011539416.1:n.15459+234_15459+238dup
XM_011541115.1:c.15453+234_15453+238dup	XP_011539417.1:n.15453+234_15453+238dup
XM_011541116.1:c.15444+234_15444+238dup	XP_011539418.1:n.15444+234_15444+238dup
XM_011541117.1:c.15393+234_15393+238dup	XP_011539419.1:n.15393+234_15393+238dup
XM_011541118.1:c.15390+234_15390+238dup	XP_011539420.1:n.15390+234_15390+238dup
XM_011541119.1:c.15357+234_15357+238dup	XP_011539421.1:n.15357+234_15357+238dup
XM_011541120.1:c.15354+234_15354+238dup	XP_011539422.1:n.15354+234_15354+238dup
XM_011541121.1:c.15321+234_15321+238dup	XP_011539423.1:n.15321+234_15321+238dup
XM_011541108.3:c.15591+234_15591+238dup	XP_011539410.2:n.15591+234_15591+238dup
XM_011541109.3:c.15588+234_15588+238dup	XP_011539411.2:n.15588+234_15588+238dup
XM_011541110.3:c.15588+234_15588+238dup	XP_011539412.2:n.15588+234_15588+238dup
XM_011541111.3:c.15588+234_15588+238dup	XP_011539413.2:n.15588+234_15588+238dup
XM_011541112.3:c.15576+234_15576+238dup	XP_011539414.2:n.15576+234_15576+238dup
XM_011541113.3:c.15573+234_15573+238dup	XP_011539415.2:n.15573+234_15573+238dup
XM_011541114.3:c.15573+234_15573+238dup	XP_011539416.2:n.15573+234_15573+238dup
XM_011541115.3:c.15567+234_15567+238dup	XP_011539417.2:n.15567+234_15567+238dup
XM_011541116.3:c.15558+234_15558+238dup	XP_011539418.2:n.15558+234_15558+238dup
XM_011541117.3:c.15507+234_15507+238dup	XP_011539419.2:n.15507+234_15507+238dup
XM_011541118.3:c.15504+234_15504+238dup	XP_011539420.2:n.15504+234_15504+238dup
XM_011541119.3:c.15471+234_15471+238dup	XP_011539421.2:n.15471+234_15471+238dup
XM_011541120.3:c.15468+234_15468+238dup	XP_011539422.2:n.15468+234_15468+238dup
XM_011541121.3:c.15435+234_15435+238dup	XP_011539423.2:n.15435+234_15435+238dup
XM_017000822.2:c.15570+234_15570+238dup	XP_016856311.2:n.15570+234_15570+238dup
XM_017000823.2:c.15543+234_15543+238dup	XP_016856312.2:n.15543+234_15543+238dup
XM_017000824.2:c.15489+234_15489+238dup	XP_016856313.2:n.15489+234_15489+238dup
XM_017000825.2:c.15474+234_15474+238dup	XP_016856314.2:n.15474+234_15474+238dup
XM_017000826.2:c.15471+234_15471+238dup	XP_016856315.2:n.15471+234_15471+238dup
XM_017000827.2:c.15456+234_15456+238dup	XP_016856316.2:n.15456+234_15456+238dup
XM_017000828.2:c.15432+234_15432+238dup	XP_016856317.2:n.15432+234_15432+238dup
XM_017000829.2:c.15384+234_15384+238dup	XP_016856318.2:n.15384+234_15384+238dup
XM_017000830.2:c.15333+234_15333+238dup	XP_016856319.2:n.15333+234_15333+238dup
NM_020765.3:c.15324+234_15324+238dup MANE Select	NP_065816.2:n.15324+234_15324+238dup