Canonical Allele Identifier: CA4896752
Gene: DENND3 HGNC NCBI

Linked Data

dbSNP Id: rs763038519

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.141168045C>T , CM000670.2:g.141168045C>T GRCh38
NC_000008.10:g.142178144C>T , CM000670.1:g.142178144C>T GRCh37
NC_000008.9:g.142247326C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000519811.6:c.1795C>T MANE Select ENSP00000428714.1:p.Pro599Ser
ENST00000262585.6:c.1555C>T ENSP00000262585.2:p.Pro519Ser
ENST00000424248.2:c.1399C>T ENSP00000410594.1:p.Pro467Ser
ENST00000518668.5:c.1568C>T
ENST00000519811.5:c.1795C>T ENSP00000428714.1:p.Pro599Ser
ENST00000520482.1:n.1336C>T
NM_014957.2:c.1555C>T NP_055772.2:p.Pro519Ser
XM_005250838.3:c.1594C>T XP_005250895.2:p.Pro532Ser
XM_005250839.2:c.1594C>T XP_005250896.2:p.Pro532Ser
XM_005250840.3:c.1438C>T XP_005250897.2:p.Pro480Ser
XM_005250841.2:c.1438C>T XP_005250898.2:p.Pro480Ser
XM_005250842.3:c.1561C>T XP_005250899.1:p.Pro521Ser
XM_005250843.3:c.1051C>T XP_005250900.1:p.Pro351Ser
XM_011516933.1:c.1594C>T XP_011515235.1:p.Pro532Ser
XM_011516934.1:c.1594C>T XP_011515236.1:p.Pro532Ser
XM_011516935.1:c.1228C>T XP_011515237.1:p.Pro410Ser
XM_011516936.1:c.1222C>T XP_011515238.1:p.Pro408Ser
XM_011516937.1:c.1594C>T XP_011515239.1:p.Pro532Ser
XM_011516938.1:c.763C>T XP_011515240.1:p.Pro255Ser
XM_011516939.1:c.292C>T XP_011515241.1:p.Pro98Ser
XM_011516940.1:c.292C>T XP_011515242.1:p.Pro98Ser
XM_011516941.1:c.1594C>T XP_011515243.1:p.Pro532Ser
XM_011516942.1:c.1594C>T XP_011515244.1:p.Pro532Ser
XR_242384.2:n.1724C>T
XR_928310.1:n.1724C>T
XR_928311.1:n.1724C>T
XR_928312.1:n.1724C>T
NM_001352890.2:c.1795C>T NP_001339819.2:p.Pro599Ser
NM_001362798.1:c.1795C>T NP_001349727.1:p.Pro599Ser
NM_014957.4:c.1594C>T NP_055772.3:p.Pro532Ser
NR_148197.2:n.1891C>T
XM_005250840.5:c.1639C>T XP_005250897.3:p.Pro547Ser
XM_005250841.4:c.1639C>T XP_005250898.3:p.Pro547Ser
XM_005250842.4:c.1561C>T XP_005250899.1:p.Pro521Ser
XM_011516933.2:c.1795C>T XP_011515235.2:p.Pro599Ser
XM_011516934.3:c.1795C>T XP_011515236.2:p.Pro599Ser
XM_011516937.2:c.1795C>T XP_011515239.2:p.Pro599Ser
XM_011516938.3:c.763C>T XP_011515240.1:p.Pro255Ser
XM_011516939.3:c.292C>T XP_011515241.1:p.Pro98Ser
XM_011516940.2:c.292C>T XP_011515242.1:p.Pro98Ser
XM_011516941.3:c.1795C>T XP_011515243.2:p.Pro599Ser
XM_017013241.1:c.1594C>T XP_016868730.1:p.Pro532Ser
XM_017013242.1:c.1051C>T XP_016868731.1:p.Pro351Ser
XM_017013243.1:c.331C>T XP_016868732.1:p.Pro111Ser
XR_001745497.2:n.1941C>T
XR_001745498.2:n.1941C>T
XR_928310.3:n.1941C>T
XR_928312.3:n.1941C>T
NM_001352890.3:c.1795C>T MANE Select NP_001339819.2:p.Pro599Ser
NM_001362798.2:c.1795C>T NP_001349727.1:p.Pro599Ser
NM_014957.5:c.1594C>T NP_055772.3:p.Pro532Ser
NR_148197.3:n.1914C>T