Canonical Allele Identifier: CA2579262219

Gene: DENND3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168118_141168120dup , CM000670.2:g.141168118_141168120dup	GRCh38
NC_000008.10:g.142178217_142178219dup , CM000670.1:g.142178217_142178219dup	GRCh37
NC_000008.9:g.142247399_142247401dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1868_1870dup MANE Select	ENSP00000428714.1:p.Glu623_Ala624insGlu
ENST00000262585.6:c.1628_1630dup	ENSP00000262585.2:p.Glu543_Ala544insGlu
ENST00000424248.2:c.1472_1474dup	ENSP00000410594.1:p.Glu491_Ala492insGlu
ENST00000518668.5:c.1641_1643dup
ENST00000519811.5:c.1868_1870dup	ENSP00000428714.1:p.Glu623_Ala624insGlu
ENST00000520482.1:n.1409_1411dup
NM_014957.2:c.1628_1630dup	NP_055772.2:p.Glu543_Ala544insGlu
XM_005250838.3:c.1667_1669dup	XP_005250895.2:p.Glu556_Ala557insGlu
XM_005250839.2:c.1667_1669dup	XP_005250896.2:p.Glu556_Ala557insGlu
XM_005250840.3:c.1511_1513dup	XP_005250897.2:p.Glu504_Ala505insGlu
XM_005250841.2:c.1511_1513dup	XP_005250898.2:p.Glu504_Ala505insGlu
XM_005250842.3:c.1634_1636dup	XP_005250899.1:p.Glu545_Ala546insGlu
XM_005250843.3:c.1124_1126dup	XP_005250900.1:p.Glu375_Ala376insGlu
XM_011516933.1:c.1667_1669dup	XP_011515235.1:p.Glu556_Ala557insGlu
XM_011516934.1:c.1667_1669dup	XP_011515236.1:p.Glu556_Ala557insGlu
XM_011516935.1:c.1301_1303dup	XP_011515237.1:p.Glu434_Ala435insGlu
XM_011516936.1:c.1295_1297dup	XP_011515238.1:p.Glu432_Ala433insGlu
XM_011516937.1:c.1667_1669dup	XP_011515239.1:p.Glu556_Ala557insGlu
XM_011516938.1:c.836_838dup	XP_011515240.1:p.Glu279_Ala280insGlu
XM_011516939.1:c.365_367dup	XP_011515241.1:p.Glu122_Ala123insGlu
XM_011516940.1:c.365_367dup	XP_011515242.1:p.Glu122_Ala123insGlu
XM_011516941.1:c.1667_1669dup	XP_011515243.1:p.Glu556_Ala557insGlu
XM_011516942.1:c.1667_1669dup	XP_011515244.1:p.Glu556_Ala557insGlu
XR_242384.2:n.1797_1799dup
XR_928310.1:n.1797_1799dup
XR_928311.1:n.1797_1799dup
XR_928312.1:n.1797_1799dup
NM_001352890.2:c.1868_1870dup	NP_001339819.2:p.Glu623_Ala624insGlu
NM_001362798.1:c.1868_1870dup	NP_001349727.1:p.Glu623_Ala624insGlu
NM_014957.4:c.1667_1669dup	NP_055772.3:p.Glu556_Ala557insGlu
NR_148197.2:n.1964_1966dup
XM_005250840.5:c.1712_1714dup	XP_005250897.3:p.Glu571_Ala572insGlu
XM_005250841.4:c.1712_1714dup	XP_005250898.3:p.Glu571_Ala572insGlu
XM_005250842.4:c.1634_1636dup	XP_005250899.1:p.Glu545_Ala546insGlu
XM_011516933.2:c.1868_1870dup	XP_011515235.2:p.Glu623_Ala624insGlu
XM_011516934.3:c.1868_1870dup	XP_011515236.2:p.Glu623_Ala624insGlu
XM_011516937.2:c.1868_1870dup	XP_011515239.2:p.Glu623_Ala624insGlu
XM_011516938.3:c.836_838dup	XP_011515240.1:p.Glu279_Ala280insGlu
XM_011516939.3:c.365_367dup	XP_011515241.1:p.Glu122_Ala123insGlu
XM_011516940.2:c.365_367dup	XP_011515242.1:p.Glu122_Ala123insGlu
XM_011516941.3:c.1868_1870dup	XP_011515243.2:p.Glu623_Ala624insGlu
XM_017013241.1:c.1667_1669dup	XP_016868730.1:p.Glu556_Ala557insGlu
XM_017013242.1:c.1124_1126dup	XP_016868731.1:p.Glu375_Ala376insGlu
XM_017013243.1:c.404_406dup	XP_016868732.1:p.Glu135_Ala136insGlu
XR_001745497.2:n.2014_2016dup
XR_001745498.2:n.2014_2016dup
XR_928310.3:n.2014_2016dup
XR_928312.3:n.2014_2016dup
NM_001352890.3:c.1868_1870dup MANE Select	NP_001339819.2:p.Glu623_Ala624insGlu
NM_001362798.2:c.1868_1870dup	NP_001349727.1:p.Glu623_Ala624insGlu
NM_014957.5:c.1667_1669dup	NP_055772.3:p.Glu556_Ala557insGlu
NR_148197.3:n.1987_1989dup