Canonical Allele Identifier: CA521499937

Gene: UBR4

Linked Data

• dbSNP Id: rs1449192664
• gnomAD v2: 1-19404369-CGGA-C
• gnomAD v3: 1-19077875-CGGA-C
• gnomAD v4: 1-19077875-CGGA-C
• MyVariant Identifiers: chr1:g.19404370_19404372del (hg19) ; chr1:g.19077876_19077878del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077880_19077882del , CM000663.2:g.19077880_19077882del	GRCh38
NC_000001.10:g.19404374_19404376del , CM000663.1:g.19404374_19404376del	GRCh37
NC_000001.9:g.19276961_19276963del	NCBI36
NG_027669.1:g.137375_137377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+98_15324+100del MANE Select	ENSP00000364403.3:n.15324+98_15324+100del
ENST00000375224.1:c.2445+98_2445+100del	ENSP00000364372.1:n.2445+98_2445+100del
ENST00000375225.7:c.549+98_549+100del	ENSP00000364373.3:n.549+98_549+100del
ENST00000375254.7:c.15324+98_15324+100del	ENSP00000364403.3:n.15324+98_15324+100del
ENST00000459947.5:n.3331+98_3331+100del
NM_020765.2:c.15324+98_15324+100del	NP_065816.2:n.15324+98_15324+100del
XM_011541108.1:c.15477+98_15477+100del	XP_011539410.1:n.15477+98_15477+100del
XM_011541109.1:c.15474+98_15474+100del	XP_011539411.1:n.15474+98_15474+100del
XM_011541110.1:c.15474+98_15474+100del	XP_011539412.1:n.15474+98_15474+100del
XM_011541111.1:c.15474+98_15474+100del	XP_011539413.1:n.15474+98_15474+100del
XM_011541112.1:c.15462+98_15462+100del	XP_011539414.1:n.15462+98_15462+100del
XM_011541113.1:c.15459+98_15459+100del	XP_011539415.1:n.15459+98_15459+100del
XM_011541114.1:c.15459+98_15459+100del	XP_011539416.1:n.15459+98_15459+100del
XM_011541115.1:c.15453+98_15453+100del	XP_011539417.1:n.15453+98_15453+100del
XM_011541116.1:c.15444+98_15444+100del	XP_011539418.1:n.15444+98_15444+100del
XM_011541117.1:c.15393+98_15393+100del	XP_011539419.1:n.15393+98_15393+100del
XM_011541118.1:c.15390+98_15390+100del	XP_011539420.1:n.15390+98_15390+100del
XM_011541119.1:c.15357+98_15357+100del	XP_011539421.1:n.15357+98_15357+100del
XM_011541120.1:c.15354+98_15354+100del	XP_011539422.1:n.15354+98_15354+100del
XM_011541121.1:c.15321+98_15321+100del	XP_011539423.1:n.15321+98_15321+100del
XM_011541108.3:c.15591+98_15591+100del	XP_011539410.2:n.15591+98_15591+100del
XM_011541109.3:c.15588+98_15588+100del	XP_011539411.2:n.15588+98_15588+100del
XM_011541110.3:c.15588+98_15588+100del	XP_011539412.2:n.15588+98_15588+100del
XM_011541111.3:c.15588+98_15588+100del	XP_011539413.2:n.15588+98_15588+100del
XM_011541112.3:c.15576+98_15576+100del	XP_011539414.2:n.15576+98_15576+100del
XM_011541113.3:c.15573+98_15573+100del	XP_011539415.2:n.15573+98_15573+100del
XM_011541114.3:c.15573+98_15573+100del	XP_011539416.2:n.15573+98_15573+100del
XM_011541115.3:c.15567+98_15567+100del	XP_011539417.2:n.15567+98_15567+100del
XM_011541116.3:c.15558+98_15558+100del	XP_011539418.2:n.15558+98_15558+100del
XM_011541117.3:c.15507+98_15507+100del	XP_011539419.2:n.15507+98_15507+100del
XM_011541118.3:c.15504+98_15504+100del	XP_011539420.2:n.15504+98_15504+100del
XM_011541119.3:c.15471+98_15471+100del	XP_011539421.2:n.15471+98_15471+100del
XM_011541120.3:c.15468+98_15468+100del	XP_011539422.2:n.15468+98_15468+100del
XM_011541121.3:c.15435+98_15435+100del	XP_011539423.2:n.15435+98_15435+100del
XM_017000822.2:c.15570+98_15570+100del	XP_016856311.2:n.15570+98_15570+100del
XM_017000823.2:c.15543+98_15543+100del	XP_016856312.2:n.15543+98_15543+100del
XM_017000824.2:c.15489+98_15489+100del	XP_016856313.2:n.15489+98_15489+100del
XM_017000825.2:c.15474+98_15474+100del	XP_016856314.2:n.15474+98_15474+100del
XM_017000826.2:c.15471+98_15471+100del	XP_016856315.2:n.15471+98_15471+100del
XM_017000827.2:c.15456+98_15456+100del	XP_016856316.2:n.15456+98_15456+100del
XM_017000828.2:c.15432+98_15432+100del	XP_016856317.2:n.15432+98_15432+100del
XM_017000829.2:c.15384+98_15384+100del	XP_016856318.2:n.15384+98_15384+100del
XM_017000830.2:c.15333+98_15333+100del	XP_016856319.2:n.15333+98_15333+100del
NM_020765.3:c.15324+98_15324+100del MANE Select	NP_065816.2:n.15324+98_15324+100del