Canonical Allele Identifier: CA2839052565
Gene: DENND3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.141168315dup , CM000670.2:g.141168315dup GRCh38
NC_000008.10:g.142178414dup , CM000670.1:g.142178414dup GRCh37
NC_000008.9:g.142247596dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000519811.6:c.2065dup MANE Select ENSP00000428714.1:p.Glu689GlyfsTer4
ENST00000262585.6:c.1825dup ENSP00000262585.2:p.Glu609GlyfsTer4
ENST00000424248.2:c.1669dup ENSP00000410594.1:p.Glu557GlyfsTer4
ENST00000518668.5:c.1838dup
ENST00000519811.5:c.2065dup ENSP00000428714.1:p.Glu689GlyfsTer4
ENST00000520482.1:n.1606dup
NM_014957.2:c.1825dup NP_055772.2:p.Glu609GlyfsTer4
XM_005250838.3:c.1864dup XP_005250895.2:p.Glu622GlyfsTer4
XM_005250839.2:c.1864dup XP_005250896.2:p.Glu622GlyfsTer4
XM_005250840.3:c.1708dup XP_005250897.2:p.Glu570GlyfsTer4
XM_005250841.2:c.1708dup XP_005250898.2:p.Glu570GlyfsTer4
XM_005250842.3:c.1831dup XP_005250899.1:p.Glu611GlyfsTer4
XM_005250843.3:c.1321dup XP_005250900.1:p.Glu441GlyfsTer4
XM_011516933.1:c.1864dup XP_011515235.1:p.Glu622GlyfsTer4
XM_011516934.1:c.1864dup XP_011515236.1:p.Glu622GlyfsTer4
XM_011516935.1:c.1498dup XP_011515237.1:p.Glu500GlyfsTer4
XM_011516936.1:c.1492dup XP_011515238.1:p.Glu498GlyfsTer4
XM_011516937.1:c.1864dup XP_011515239.1:p.Glu622GlyfsTer4
XM_011516938.1:c.1033dup XP_011515240.1:p.Glu345GlyfsTer4
XM_011516939.1:c.562dup XP_011515241.1:p.Glu188GlyfsTer4
XM_011516940.1:c.562dup XP_011515242.1:p.Glu188GlyfsTer4
XM_011516941.1:c.1864dup XP_011515243.1:p.Glu622GlyfsTer4
XM_011516942.1:c.1864dup XP_011515244.1:p.Glu622GlyfsTer4
XR_242384.2:n.1994dup
XR_928310.1:n.1994dup
XR_928311.1:n.1994dup
XR_928312.1:n.1994dup
NM_001352890.2:c.2065dup NP_001339819.2:p.Glu689GlyfsTer4
NM_001362798.1:c.2065dup NP_001349727.1:p.Glu689GlyfsTer4
NM_014957.4:c.1864dup NP_055772.3:p.Glu622GlyfsTer4
NR_148197.2:n.2161dup
XM_005250840.5:c.1909dup XP_005250897.3:p.Glu637GlyfsTer4
XM_005250841.4:c.1909dup XP_005250898.3:p.Glu637GlyfsTer4
XM_005250842.4:c.1831dup XP_005250899.1:p.Glu611GlyfsTer4
XM_011516933.2:c.2065dup XP_011515235.2:p.Glu689GlyfsTer4
XM_011516934.3:c.2065dup XP_011515236.2:p.Glu689GlyfsTer4
XM_011516937.2:c.2065dup XP_011515239.2:p.Glu689GlyfsTer4
XM_011516938.3:c.1033dup XP_011515240.1:p.Glu345GlyfsTer4
XM_011516939.3:c.562dup XP_011515241.1:p.Glu188GlyfsTer4
XM_011516940.2:c.562dup XP_011515242.1:p.Glu188GlyfsTer4
XM_011516941.3:c.2065dup XP_011515243.2:p.Glu689GlyfsTer4
XM_017013241.1:c.1864dup XP_016868730.1:p.Glu622GlyfsTer4
XM_017013242.1:c.1321dup XP_016868731.1:p.Glu441GlyfsTer4
XM_017013243.1:c.601dup XP_016868732.1:p.Glu201GlyfsTer4
XR_001745497.2:n.2211dup
XR_001745498.2:n.2211dup
XR_928310.3:n.2211dup
XR_928312.3:n.2211dup
NM_001352890.3:c.2065dup MANE Select NP_001339819.2:p.Glu689GlyfsTer4
NM_001362798.2:c.2065dup NP_001349727.1:p.Glu689GlyfsTer4
NM_014957.5:c.1864dup NP_055772.3:p.Glu622GlyfsTer4
NR_148197.3:n.2184dup