Canonical Allele Identifier: CA645558844

Gene: DENND3

Linked Data

• COSMIC: COSM5835510

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168067_141168068insC , CM000670.2:g.141168067_141168068insC	GRCh38
NC_000008.10:g.142178166_142178167insC , CM000670.1:g.142178166_142178167insC	GRCh37
NC_000008.9:g.142247348_142247349insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1817_1818insC MANE Select	ENSP00000428714.1:p.Glu606AspfsTer27
ENST00000262585.6:c.1577_1578insC	ENSP00000262585.2:p.Glu526AspfsTer27
ENST00000424248.2:c.1421_1422insC	ENSP00000410594.1:p.Glu474AspfsTer27
ENST00000518668.5:c.1590_1591insC
ENST00000519811.5:c.1817_1818insC	ENSP00000428714.1:p.Glu606AspfsTer27
ENST00000520482.1:n.1358_1359insC
NM_014957.2:c.1577_1578insC	NP_055772.2:p.Glu526AspfsTer27
XM_005250838.3:c.1616_1617insC	XP_005250895.2:p.Glu539AspfsTer27
XM_005250839.2:c.1616_1617insC	XP_005250896.2:p.Glu539AspfsTer27
XM_005250840.3:c.1460_1461insC	XP_005250897.2:p.Glu487AspfsTer27
XM_005250841.2:c.1460_1461insC	XP_005250898.2:p.Glu487AspfsTer27
XM_005250842.3:c.1583_1584insC	XP_005250899.1:p.Glu528AspfsTer27
XM_005250843.3:c.1073_1074insC	XP_005250900.1:p.Glu358AspfsTer27
XM_011516933.1:c.1616_1617insC	XP_011515235.1:p.Glu539AspfsTer27
XM_011516934.1:c.1616_1617insC	XP_011515236.1:p.Glu539AspfsTer27
XM_011516935.1:c.1250_1251insC	XP_011515237.1:p.Glu417AspfsTer27
XM_011516936.1:c.1244_1245insC	XP_011515238.1:p.Glu415AspfsTer27
XM_011516937.1:c.1616_1617insC	XP_011515239.1:p.Glu539AspfsTer27
XM_011516938.1:c.785_786insC	XP_011515240.1:p.Glu262AspfsTer27
XM_011516939.1:c.314_315insC	XP_011515241.1:p.Glu105AspfsTer27
XM_011516940.1:c.314_315insC	XP_011515242.1:p.Glu105AspfsTer27
XM_011516941.1:c.1616_1617insC	XP_011515243.1:p.Glu539AspfsTer27
XM_011516942.1:c.1616_1617insC	XP_011515244.1:p.Glu539AspfsTer27
XR_242384.2:n.1746_1747insC
XR_928310.1:n.1746_1747insC
XR_928311.1:n.1746_1747insC
XR_928312.1:n.1746_1747insC
NM_001352890.2:c.1817_1818insC	NP_001339819.2:p.Glu606AspfsTer27
NM_001362798.1:c.1817_1818insC	NP_001349727.1:p.Glu606AspfsTer27
NM_014957.4:c.1616_1617insC	NP_055772.3:p.Glu539AspfsTer27
NR_148197.2:n.1913_1914insC
XM_005250840.5:c.1661_1662insC	XP_005250897.3:p.Glu554AspfsTer27
XM_005250841.4:c.1661_1662insC	XP_005250898.3:p.Glu554AspfsTer27
XM_005250842.4:c.1583_1584insC	XP_005250899.1:p.Glu528AspfsTer27
XM_011516933.2:c.1817_1818insC	XP_011515235.2:p.Glu606AspfsTer27
XM_011516934.3:c.1817_1818insC	XP_011515236.2:p.Glu606AspfsTer27
XM_011516937.2:c.1817_1818insC	XP_011515239.2:p.Glu606AspfsTer27
XM_011516938.3:c.785_786insC	XP_011515240.1:p.Glu262AspfsTer27
XM_011516939.3:c.314_315insC	XP_011515241.1:p.Glu105AspfsTer27
XM_011516940.2:c.314_315insC	XP_011515242.1:p.Glu105AspfsTer27
XM_011516941.3:c.1817_1818insC	XP_011515243.2:p.Glu606AspfsTer27
XM_017013241.1:c.1616_1617insC	XP_016868730.1:p.Glu539AspfsTer27
XM_017013242.1:c.1073_1074insC	XP_016868731.1:p.Glu358AspfsTer27
XM_017013243.1:c.353_354insC	XP_016868732.1:p.Glu118AspfsTer27
XR_001745497.2:n.1963_1964insC
XR_001745498.2:n.1963_1964insC
XR_928310.3:n.1963_1964insC
XR_928312.3:n.1963_1964insC
NM_001352890.3:c.1817_1818insC MANE Select	NP_001339819.2:p.Glu606AspfsTer27
NM_001362798.2:c.1817_1818insC	NP_001349727.1:p.Glu606AspfsTer27
NM_014957.5:c.1616_1617insC	NP_055772.3:p.Glu539AspfsTer27
NR_148197.3:n.1936_1937insC