Canonical Allele Identifier: CA16044030
Gene: DENND3 HGNC NCBI

Linked Data

ClinVar Variation Id: 375278
ClinVar RCV Id: RCV000416370
dbSNP Id: rs1057519052

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.141168410del , CM000670.2:g.141168410del GRCh38
NC_000008.10:g.142178509del , CM000670.1:g.142178509del GRCh37
NC_000008.9:g.142247691del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000519811.6:c.2160del MANE Select ENSP00000428714.1:p.Lys720AsnfsTer15
ENST00000262585.6:c.1920del ENSP00000262585.2:p.Lys640AsnfsTer15
ENST00000424248.2:c.1764del ENSP00000410594.1:p.Lys588AsnfsTer15
ENST00000518668.5:c.1933del
ENST00000519811.5:c.2160del ENSP00000428714.1:p.Lys720AsnfsTer15
ENST00000520482.1:n.1701del
NM_014957.2:c.1920del NP_055772.2:p.Lys640AsnfsTer15
XM_005250838.3:c.1959del XP_005250895.2:p.Lys653AsnfsTer15
XM_005250839.2:c.1959del XP_005250896.2:p.Lys653AsnfsTer15
XM_005250840.3:c.1803del XP_005250897.2:p.Lys601AsnfsTer15
XM_005250841.2:c.1803del XP_005250898.2:p.Lys601AsnfsTer15
XM_005250842.3:c.1926del XP_005250899.1:p.Lys642AsnfsTer15
XM_005250843.3:c.1416del XP_005250900.1:p.Lys472AsnfsTer15
XM_011516933.1:c.1959del XP_011515235.1:p.Lys653AsnfsTer15
XM_011516934.1:c.1959del XP_011515236.1:p.Lys653AsnfsTer15
XM_011516935.1:c.1593del XP_011515237.1:p.Lys531AsnfsTer15
XM_011516936.1:c.1587del XP_011515238.1:p.Lys529AsnfsTer15
XM_011516937.1:c.1959del XP_011515239.1:p.Lys653AsnfsTer15
XM_011516938.1:c.1128del XP_011515240.1:p.Lys376AsnfsTer15
XM_011516939.1:c.657del XP_011515241.1:p.Lys219AsnfsTer15
XM_011516940.1:c.657del XP_011515242.1:p.Lys219AsnfsTer15
XM_011516941.1:c.1959del XP_011515243.1:p.Lys653AsnfsTer15
XM_011516942.1:c.1959del XP_011515244.1:p.Lys653AsnfsTer15
XR_242384.2:n.2089del
XR_928310.1:n.2089del
XR_928311.1:n.2089del
XR_928312.1:n.2089del
NM_001352890.2:c.2160del NP_001339819.2:p.Lys720AsnfsTer15
NM_001362798.1:c.2160del NP_001349727.1:p.Lys720AsnfsTer15
NM_014957.4:c.1959del NP_055772.3:p.Lys653AsnfsTer15
NR_148197.2:n.2256del
XM_005250840.5:c.2004del XP_005250897.3:p.Lys668AsnfsTer15
XM_005250841.4:c.2004del XP_005250898.3:p.Lys668AsnfsTer15
XM_005250842.4:c.1926del XP_005250899.1:p.Lys642AsnfsTer15
XM_011516933.2:c.2160del XP_011515235.2:p.Lys720AsnfsTer15
XM_011516934.3:c.2160del XP_011515236.2:p.Lys720AsnfsTer15
XM_011516937.2:c.2160del XP_011515239.2:p.Lys720AsnfsTer15
XM_011516938.3:c.1128del XP_011515240.1:p.Lys376AsnfsTer15
XM_011516939.3:c.657del XP_011515241.1:p.Lys219AsnfsTer15
XM_011516940.2:c.657del XP_011515242.1:p.Lys219AsnfsTer15
XM_011516941.3:c.2160del XP_011515243.2:p.Lys720AsnfsTer15
XM_017013241.1:c.1959del XP_016868730.1:p.Lys653AsnfsTer15
XM_017013242.1:c.1416del XP_016868731.1:p.Lys472AsnfsTer15
XM_017013243.1:c.696del XP_016868732.1:p.Lys232AsnfsTer15
XR_001745497.2:n.2306del
XR_001745498.2:n.2306del
XR_928310.3:n.2306del
XR_928312.3:n.2306del
NM_001352890.3:c.2160del MANE Select NP_001339819.2:p.Lys720AsnfsTer15
NM_001362798.2:c.2160del NP_001349727.1:p.Lys720AsnfsTer15
NM_014957.5:c.1959del NP_055772.3:p.Lys653AsnfsTer15
NR_148197.3:n.2279del