Canonical Allele Identifier: CA372344354
Gene: DENND3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.141168412T>C , CM000670.2:g.141168412T>C GRCh38
NC_000008.10:g.142178511T>C , CM000670.1:g.142178511T>C GRCh37
NC_000008.9:g.142247693T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000519811.6:c.2162T>C MANE Select ENSP00000428714.1:p.Phe721Ser
ENST00000262585.6:c.1922T>C ENSP00000262585.2:p.Phe641Ser
ENST00000424248.2:c.1766T>C ENSP00000410594.1:p.Phe589Ser
ENST00000518668.5:c.1935T>C
ENST00000519811.5:c.2162T>C ENSP00000428714.1:p.Phe721Ser
ENST00000520482.1:n.1703T>C
NM_014957.2:c.1922T>C NP_055772.2:p.Phe641Ser
XM_005250838.3:c.1961T>C XP_005250895.2:p.Phe654Ser
XM_005250839.2:c.1961T>C XP_005250896.2:p.Phe654Ser
XM_005250840.3:c.1805T>C XP_005250897.2:p.Phe602Ser
XM_005250841.2:c.1805T>C XP_005250898.2:p.Phe602Ser
XM_005250842.3:c.1928T>C XP_005250899.1:p.Phe643Ser
XM_005250843.3:c.1418T>C XP_005250900.1:p.Phe473Ser
XM_011516933.1:c.1961T>C XP_011515235.1:p.Phe654Ser
XM_011516934.1:c.1961T>C XP_011515236.1:p.Phe654Ser
XM_011516935.1:c.1595T>C XP_011515237.1:p.Phe532Ser
XM_011516936.1:c.1589T>C XP_011515238.1:p.Phe530Ser
XM_011516937.1:c.1961T>C XP_011515239.1:p.Phe654Ser
XM_011516938.1:c.1130T>C XP_011515240.1:p.Phe377Ser
XM_011516939.1:c.659T>C XP_011515241.1:p.Phe220Ser
XM_011516940.1:c.659T>C XP_011515242.1:p.Phe220Ser
XM_011516941.1:c.1961T>C XP_011515243.1:p.Phe654Ser
XM_011516942.1:c.1961T>C XP_011515244.1:p.Phe654Ser
XR_242384.2:n.2091T>C
XR_928310.1:n.2091T>C
XR_928311.1:n.2091T>C
XR_928312.1:n.2091T>C
NM_001352890.2:c.2162T>C NP_001339819.2:p.Phe721Ser
NM_001362798.1:c.2162T>C NP_001349727.1:p.Phe721Ser
NM_014957.4:c.1961T>C NP_055772.3:p.Phe654Ser
NR_148197.2:n.2258T>C
XM_005250840.5:c.2006T>C XP_005250897.3:p.Phe669Ser
XM_005250841.4:c.2006T>C XP_005250898.3:p.Phe669Ser
XM_005250842.4:c.1928T>C XP_005250899.1:p.Phe643Ser
XM_011516933.2:c.2162T>C XP_011515235.2:p.Phe721Ser
XM_011516934.3:c.2162T>C XP_011515236.2:p.Phe721Ser
XM_011516937.2:c.2162T>C XP_011515239.2:p.Phe721Ser
XM_011516938.3:c.1130T>C XP_011515240.1:p.Phe377Ser
XM_011516939.3:c.659T>C XP_011515241.1:p.Phe220Ser
XM_011516940.2:c.659T>C XP_011515242.1:p.Phe220Ser
XM_011516941.3:c.2162T>C XP_011515243.2:p.Phe721Ser
XM_017013241.1:c.1961T>C XP_016868730.1:p.Phe654Ser
XM_017013242.1:c.1418T>C XP_016868731.1:p.Phe473Ser
XM_017013243.1:c.698T>C XP_016868732.1:p.Phe233Ser
XR_001745497.2:n.2308T>C
XR_001745498.2:n.2308T>C
XR_928310.3:n.2308T>C
XR_928312.3:n.2308T>C
NM_001352890.3:c.2162T>C MANE Select NP_001339819.2:p.Phe721Ser
NM_001362798.2:c.2162T>C NP_001349727.1:p.Phe721Ser
NM_014957.5:c.1961T>C NP_055772.3:p.Phe654Ser
NR_148197.3:n.2281T>C