Canonical Allele Identifier: CA2688780441

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168444-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168445del , CM000670.2:g.141168445del	GRCh38
NC_000008.10:g.142178544del , CM000670.1:g.142178544del	GRCh37
NC_000008.9:g.142247726del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2195del MANE Select	ENSP00000428714.1:p.Asp732AlafsTer3
ENST00000262585.6:c.1955del	ENSP00000262585.2:p.Asp652AlafsTer3
ENST00000424248.2:c.1799del	ENSP00000410594.1:p.Asp600AlafsTer3
ENST00000518668.5:c.1968del
ENST00000519811.5:c.2195del	ENSP00000428714.1:p.Asp732AlafsTer3
ENST00000520482.1:n.1736del
NM_014957.2:c.1955del	NP_055772.2:p.Asp652AlafsTer3
XM_005250838.3:c.1994del	XP_005250895.2:p.Asp665AlafsTer3
XM_005250839.2:c.1994del	XP_005250896.2:p.Asp665AlafsTer3
XM_005250840.3:c.1838del	XP_005250897.2:p.Asp613AlafsTer3
XM_005250841.2:c.1838del	XP_005250898.2:p.Asp613AlafsTer3
XM_005250842.3:c.1961del	XP_005250899.1:p.Asp654AlafsTer3
XM_005250843.3:c.1451del	XP_005250900.1:p.Asp484AlafsTer3
XM_011516933.1:c.1994del	XP_011515235.1:p.Asp665AlafsTer3
XM_011516934.1:c.1994del	XP_011515236.1:p.Asp665AlafsTer3
XM_011516935.1:c.1628del	XP_011515237.1:p.Asp543AlafsTer3
XM_011516936.1:c.1622del	XP_011515238.1:p.Asp541AlafsTer3
XM_011516937.1:c.1994del	XP_011515239.1:p.Asp665AlafsTer3
XM_011516938.1:c.1163del	XP_011515240.1:p.Asp388AlafsTer3
XM_011516939.1:c.692del	XP_011515241.1:p.Asp231AlafsTer3
XM_011516940.1:c.692del	XP_011515242.1:p.Asp231AlafsTer3
XM_011516941.1:c.1994del	XP_011515243.1:p.Asp665AlafsTer3
XM_011516942.1:c.1994del	XP_011515244.1:p.Asp665AlafsTer3
XR_242384.2:n.2124del
XR_928310.1:n.2124del
XR_928311.1:n.2124del
XR_928312.1:n.2124del
NM_001352890.2:c.2195del	NP_001339819.2:p.Asp732AlafsTer3
NM_001362798.1:c.2195del	NP_001349727.1:p.Asp732AlafsTer3
NM_014957.4:c.1994del	NP_055772.3:p.Asp665AlafsTer3
NR_148197.2:n.2291del
XM_005250840.5:c.2039del	XP_005250897.3:p.Asp680AlafsTer3
XM_005250841.4:c.2039del	XP_005250898.3:p.Asp680AlafsTer3
XM_005250842.4:c.1961del	XP_005250899.1:p.Asp654AlafsTer3
XM_011516933.2:c.2195del	XP_011515235.2:p.Asp732AlafsTer3
XM_011516934.3:c.2195del	XP_011515236.2:p.Asp732AlafsTer3
XM_011516937.2:c.2195del	XP_011515239.2:p.Asp732AlafsTer3
XM_011516938.3:c.1163del	XP_011515240.1:p.Asp388AlafsTer3
XM_011516939.3:c.692del	XP_011515241.1:p.Asp231AlafsTer3
XM_011516940.2:c.692del	XP_011515242.1:p.Asp231AlafsTer3
XM_011516941.3:c.2195del	XP_011515243.2:p.Asp732AlafsTer3
XM_017013241.1:c.1994del	XP_016868730.1:p.Asp665AlafsTer3
XM_017013242.1:c.1451del	XP_016868731.1:p.Asp484AlafsTer3
XM_017013243.1:c.731del	XP_016868732.1:p.Asp244AlafsTer3
XR_001745497.2:n.2341del
XR_001745498.2:n.2341del
XR_928310.3:n.2341del
XR_928312.3:n.2341del
NM_001352890.3:c.2195del MANE Select	NP_001339819.2:p.Asp732AlafsTer3
NM_001362798.2:c.2195del	NP_001349727.1:p.Asp732AlafsTer3
NM_014957.5:c.1994del	NP_055772.3:p.Asp665AlafsTer3
NR_148197.3:n.2314del