Canonical Allele Identifier: CA2688779826

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168029-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168030dup , CM000670.2:g.141168030dup	GRCh38
NC_000008.10:g.142178129dup , CM000670.1:g.142178129dup	GRCh37
NC_000008.9:g.142247311dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1780dup MANE Select	ENSP00000428714.1:p.Tyr594LeufsTer?
ENST00000262585.6:c.1540dup	ENSP00000262585.2:p.Tyr514LeufsTer?
ENST00000424248.2:c.1384dup	ENSP00000410594.1:p.Tyr462LeufsTer?
ENST00000518668.5:c.1553dup
ENST00000519811.5:c.1780dup	ENSP00000428714.1:p.Tyr594LeufsTer?
ENST00000520482.1:n.1321dup
NM_014957.2:c.1540dup	NP_055772.2:p.Tyr514LeufsTer?
XM_005250838.3:c.1579dup	XP_005250895.2:p.Tyr527LeufsTer?
XM_005250839.2:c.1579dup	XP_005250896.2:p.Tyr527LeufsTer?
XM_005250840.3:c.1423dup	XP_005250897.2:p.Tyr475LeufsTer?
XM_005250841.2:c.1423dup	XP_005250898.2:p.Tyr475LeufsTer?
XM_005250842.3:c.1546dup	XP_005250899.1:p.Tyr516LeufsTer?
XM_005250843.3:c.1036dup	XP_005250900.1:p.Tyr346LeufsTer?
XM_011516933.1:c.1579dup	XP_011515235.1:p.Tyr527LeufsTer?
XM_011516934.1:c.1579dup	XP_011515236.1:p.Tyr527LeufsTer?
XM_011516935.1:c.1213dup	XP_011515237.1:p.Tyr405LeufsTer?
XM_011516936.1:c.1207dup	XP_011515238.1:p.Tyr403LeufsTer?
XM_011516937.1:c.1579dup	XP_011515239.1:p.Tyr527LeufsTer?
XM_011516938.1:c.748dup	XP_011515240.1:p.Tyr250LeufsTer?
XM_011516939.1:c.277dup	XP_011515241.1:p.Tyr93LeufsTer?
XM_011516940.1:c.277dup	XP_011515242.1:p.Tyr93LeufsTer?
XM_011516941.1:c.1579dup	XP_011515243.1:p.Tyr527LeufsTer?
XM_011516942.1:c.1579dup	XP_011515244.1:p.Tyr527LeufsTer?
XR_242384.2:n.1709dup
XR_928310.1:n.1709dup
XR_928311.1:n.1709dup
XR_928312.1:n.1709dup
NM_001352890.2:c.1780dup	NP_001339819.2:p.Tyr594LeufsTer?
NM_001362798.1:c.1780dup	NP_001349727.1:p.Tyr594LeufsTer?
NM_014957.4:c.1579dup	NP_055772.3:p.Tyr527LeufsTer?
NR_148197.2:n.1876dup
XM_005250840.5:c.1624dup	XP_005250897.3:p.Tyr542LeufsTer?
XM_005250841.4:c.1624dup	XP_005250898.3:p.Tyr542LeufsTer?
XM_005250842.4:c.1546dup	XP_005250899.1:p.Tyr516LeufsTer?
XM_011516933.2:c.1780dup	XP_011515235.2:p.Tyr594LeufsTer?
XM_011516934.3:c.1780dup	XP_011515236.2:p.Tyr594LeufsTer?
XM_011516937.2:c.1780dup	XP_011515239.2:p.Tyr594LeufsTer?
XM_011516938.3:c.748dup	XP_011515240.1:p.Tyr250LeufsTer?
XM_011516939.3:c.277dup	XP_011515241.1:p.Tyr93LeufsTer?
XM_011516940.2:c.277dup	XP_011515242.1:p.Tyr93LeufsTer?
XM_011516941.3:c.1780dup	XP_011515243.2:p.Tyr594LeufsTer?
XM_017013241.1:c.1579dup	XP_016868730.1:p.Tyr527LeufsTer?
XM_017013242.1:c.1036dup	XP_016868731.1:p.Tyr346LeufsTer?
XM_017013243.1:c.316dup	XP_016868732.1:p.Tyr106LeufsTer?
XR_001745497.2:n.1926dup
XR_001745498.2:n.1926dup
XR_928310.3:n.1926dup
XR_928312.3:n.1926dup
NM_001352890.3:c.1780dup MANE Select	NP_001339819.2:p.Tyr594LeufsTer?
NM_001362798.2:c.1780dup	NP_001349727.1:p.Tyr594LeufsTer?
NM_014957.5:c.1579dup	NP_055772.3:p.Tyr527LeufsTer?
NR_148197.3:n.1899dup