Canonical Allele Identifier: CA2688779943

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168084-G-GCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168085_141168087dup , CM000670.2:g.141168085_141168087dup	GRCh38
NC_000008.10:g.142178184_142178186dup , CM000670.1:g.142178184_142178186dup	GRCh37
NC_000008.9:g.142247366_142247368dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1835_1837dup MANE Select	ENSP00000428714.1:p.Ala612_Tyr613insSer
ENST00000262585.6:c.1595_1597dup	ENSP00000262585.2:p.Ala532_Tyr533insSer
ENST00000424248.2:c.1439_1441dup	ENSP00000410594.1:p.Ala480_Tyr481insSer
ENST00000518668.5:c.1608_1610dup
ENST00000519811.5:c.1835_1837dup	ENSP00000428714.1:p.Ala612_Tyr613insSer
ENST00000520482.1:n.1376_1378dup
NM_014957.2:c.1595_1597dup	NP_055772.2:p.Ala532_Tyr533insSer
XM_005250838.3:c.1634_1636dup	XP_005250895.2:p.Ala545_Tyr546insSer
XM_005250839.2:c.1634_1636dup	XP_005250896.2:p.Ala545_Tyr546insSer
XM_005250840.3:c.1478_1480dup	XP_005250897.2:p.Ala493_Tyr494insSer
XM_005250841.2:c.1478_1480dup	XP_005250898.2:p.Ala493_Tyr494insSer
XM_005250842.3:c.1601_1603dup	XP_005250899.1:p.Ala534_Tyr535insSer
XM_005250843.3:c.1091_1093dup	XP_005250900.1:p.Ala364_Tyr365insSer
XM_011516933.1:c.1634_1636dup	XP_011515235.1:p.Ala545_Tyr546insSer
XM_011516934.1:c.1634_1636dup	XP_011515236.1:p.Ala545_Tyr546insSer
XM_011516935.1:c.1268_1270dup	XP_011515237.1:p.Ala423_Tyr424insSer
XM_011516936.1:c.1262_1264dup	XP_011515238.1:p.Ala421_Tyr422insSer
XM_011516937.1:c.1634_1636dup	XP_011515239.1:p.Ala545_Tyr546insSer
XM_011516938.1:c.803_805dup	XP_011515240.1:p.Ala268_Tyr269insSer
XM_011516939.1:c.332_334dup	XP_011515241.1:p.Ala111_Tyr112insSer
XM_011516940.1:c.332_334dup	XP_011515242.1:p.Ala111_Tyr112insSer
XM_011516941.1:c.1634_1636dup	XP_011515243.1:p.Ala545_Tyr546insSer
XM_011516942.1:c.1634_1636dup	XP_011515244.1:p.Ala545_Tyr546insSer
XR_242384.2:n.1764_1766dup
XR_928310.1:n.1764_1766dup
XR_928311.1:n.1764_1766dup
XR_928312.1:n.1764_1766dup
NM_001352890.2:c.1835_1837dup	NP_001339819.2:p.Ala612_Tyr613insSer
NM_001362798.1:c.1835_1837dup	NP_001349727.1:p.Ala612_Tyr613insSer
NM_014957.4:c.1634_1636dup	NP_055772.3:p.Ala545_Tyr546insSer
NR_148197.2:n.1931_1933dup
XM_005250840.5:c.1679_1681dup	XP_005250897.3:p.Ala560_Tyr561insSer
XM_005250841.4:c.1679_1681dup	XP_005250898.3:p.Ala560_Tyr561insSer
XM_005250842.4:c.1601_1603dup	XP_005250899.1:p.Ala534_Tyr535insSer
XM_011516933.2:c.1835_1837dup	XP_011515235.2:p.Ala612_Tyr613insSer
XM_011516934.3:c.1835_1837dup	XP_011515236.2:p.Ala612_Tyr613insSer
XM_011516937.2:c.1835_1837dup	XP_011515239.2:p.Ala612_Tyr613insSer
XM_011516938.3:c.803_805dup	XP_011515240.1:p.Ala268_Tyr269insSer
XM_011516939.3:c.332_334dup	XP_011515241.1:p.Ala111_Tyr112insSer
XM_011516940.2:c.332_334dup	XP_011515242.1:p.Ala111_Tyr112insSer
XM_011516941.3:c.1835_1837dup	XP_011515243.2:p.Ala612_Tyr613insSer
XM_017013241.1:c.1634_1636dup	XP_016868730.1:p.Ala545_Tyr546insSer
XM_017013242.1:c.1091_1093dup	XP_016868731.1:p.Ala364_Tyr365insSer
XM_017013243.1:c.371_373dup	XP_016868732.1:p.Ala124_Tyr125insSer
XR_001745497.2:n.1981_1983dup
XR_001745498.2:n.1981_1983dup
XR_928310.3:n.1981_1983dup
XR_928312.3:n.1981_1983dup
NM_001352890.3:c.1835_1837dup MANE Select	NP_001339819.2:p.Ala612_Tyr613insSer
NM_001362798.2:c.1835_1837dup	NP_001349727.1:p.Ala612_Tyr613insSer
NM_014957.5:c.1634_1636dup	NP_055772.3:p.Ala545_Tyr546insSer
NR_148197.3:n.1954_1956dup