Canonical Allele Identifier: CA521499917

Gene: UBR4

Linked Data

• dbSNP Id: rs1409147232
• gnomAD v2: 1-19404331-GTTGT-G
• gnomAD v4: 1-19077837-GTTGT-G
• MyVariant Identifiers: chr1:g.19404332_19404335del (hg19) ; chr1:g.19077838_19077841del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077844_19077847del , CM000663.2:g.19077844_19077847del	GRCh38
NC_000001.10:g.19404338_19404341del , CM000663.1:g.19404338_19404341del	GRCh37
NC_000001.9:g.19276925_19276928del	NCBI36
NG_027669.1:g.137412_137415del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15324+135_15324+138del MANE Select	ENSP00000364403.3:n.15324+135_15324+138del
ENST00000375224.1:c.2445+135_2445+138del	ENSP00000364372.1:n.2445+135_2445+138del
ENST00000375225.7:c.549+135_549+138del	ENSP00000364373.3:n.549+135_549+138del
ENST00000375254.7:c.15324+135_15324+138del	ENSP00000364403.3:n.15324+135_15324+138del
ENST00000459947.5:n.3331+135_3331+138del
NM_020765.2:c.15324+135_15324+138del	NP_065816.2:n.15324+135_15324+138del
XM_011541108.1:c.15477+135_15477+138del	XP_011539410.1:n.15477+135_15477+138del
XM_011541109.1:c.15474+135_15474+138del	XP_011539411.1:n.15474+135_15474+138del
XM_011541110.1:c.15474+135_15474+138del	XP_011539412.1:n.15474+135_15474+138del
XM_011541111.1:c.15474+135_15474+138del	XP_011539413.1:n.15474+135_15474+138del
XM_011541112.1:c.15462+135_15462+138del	XP_011539414.1:n.15462+135_15462+138del
XM_011541113.1:c.15459+135_15459+138del	XP_011539415.1:n.15459+135_15459+138del
XM_011541114.1:c.15459+135_15459+138del	XP_011539416.1:n.15459+135_15459+138del
XM_011541115.1:c.15453+135_15453+138del	XP_011539417.1:n.15453+135_15453+138del
XM_011541116.1:c.15444+135_15444+138del	XP_011539418.1:n.15444+135_15444+138del
XM_011541117.1:c.15393+135_15393+138del	XP_011539419.1:n.15393+135_15393+138del
XM_011541118.1:c.15390+135_15390+138del	XP_011539420.1:n.15390+135_15390+138del
XM_011541119.1:c.15357+135_15357+138del	XP_011539421.1:n.15357+135_15357+138del
XM_011541120.1:c.15354+135_15354+138del	XP_011539422.1:n.15354+135_15354+138del
XM_011541121.1:c.15321+135_15321+138del	XP_011539423.1:n.15321+135_15321+138del
XM_011541108.3:c.15591+135_15591+138del	XP_011539410.2:n.15591+135_15591+138del
XM_011541109.3:c.15588+135_15588+138del	XP_011539411.2:n.15588+135_15588+138del
XM_011541110.3:c.15588+135_15588+138del	XP_011539412.2:n.15588+135_15588+138del
XM_011541111.3:c.15588+135_15588+138del	XP_011539413.2:n.15588+135_15588+138del
XM_011541112.3:c.15576+135_15576+138del	XP_011539414.2:n.15576+135_15576+138del
XM_011541113.3:c.15573+135_15573+138del	XP_011539415.2:n.15573+135_15573+138del
XM_011541114.3:c.15573+135_15573+138del	XP_011539416.2:n.15573+135_15573+138del
XM_011541115.3:c.15567+135_15567+138del	XP_011539417.2:n.15567+135_15567+138del
XM_011541116.3:c.15558+135_15558+138del	XP_011539418.2:n.15558+135_15558+138del
XM_011541117.3:c.15507+135_15507+138del	XP_011539419.2:n.15507+135_15507+138del
XM_011541118.3:c.15504+135_15504+138del	XP_011539420.2:n.15504+135_15504+138del
XM_011541119.3:c.15471+135_15471+138del	XP_011539421.2:n.15471+135_15471+138del
XM_011541120.3:c.15468+135_15468+138del	XP_011539422.2:n.15468+135_15468+138del
XM_011541121.3:c.15435+135_15435+138del	XP_011539423.2:n.15435+135_15435+138del
XM_017000822.2:c.15570+135_15570+138del	XP_016856311.2:n.15570+135_15570+138del
XM_017000823.2:c.15543+135_15543+138del	XP_016856312.2:n.15543+135_15543+138del
XM_017000824.2:c.15489+135_15489+138del	XP_016856313.2:n.15489+135_15489+138del
XM_017000825.2:c.15474+135_15474+138del	XP_016856314.2:n.15474+135_15474+138del
XM_017000826.2:c.15471+135_15471+138del	XP_016856315.2:n.15471+135_15471+138del
XM_017000827.2:c.15456+135_15456+138del	XP_016856316.2:n.15456+135_15456+138del
XM_017000828.2:c.15432+135_15432+138del	XP_016856317.2:n.15432+135_15432+138del
XM_017000829.2:c.15384+135_15384+138del	XP_016856318.2:n.15384+135_15384+138del
XM_017000830.2:c.15333+135_15333+138del	XP_016856319.2:n.15333+135_15333+138del
NM_020765.3:c.15324+135_15324+138del MANE Select	NP_065816.2:n.15324+135_15324+138del