Canonical Allele Identifier: CA2688780424

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168386-GAAGCTGGACGACCACGTGAAGAAGTTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168393_141168419del , CM000670.2:g.141168393_141168419del	GRCh38
NC_000008.10:g.142178492_142178518del , CM000670.1:g.142178492_142178518del	GRCh37
NC_000008.9:g.142247674_142247700del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2143_2169del MANE Select	ENSP00000428714.1:p.Asp715_Leu723del
ENST00000262585.6:c.1903_1929del	ENSP00000262585.2:p.Asp635_Leu643del
ENST00000424248.2:c.1747_1773del	ENSP00000410594.1:p.Asp583_Leu591del
ENST00000518668.5:c.1916_1942del
ENST00000519811.5:c.2143_2169del	ENSP00000428714.1:p.Asp715_Leu723del
ENST00000520482.1:n.1684_1710del
NM_014957.2:c.1903_1929del	NP_055772.2:p.Asp635_Leu643del
XM_005250838.3:c.1942_1968del	XP_005250895.2:p.Asp648_Leu656del
XM_005250839.2:c.1942_1968del	XP_005250896.2:p.Asp648_Leu656del
XM_005250840.3:c.1786_1812del	XP_005250897.2:p.Asp596_Leu604del
XM_005250841.2:c.1786_1812del	XP_005250898.2:p.Asp596_Leu604del
XM_005250842.3:c.1909_1935del	XP_005250899.1:p.Asp637_Leu645del
XM_005250843.3:c.1399_1425del	XP_005250900.1:p.Asp467_Leu475del
XM_011516933.1:c.1942_1968del	XP_011515235.1:p.Asp648_Leu656del
XM_011516934.1:c.1942_1968del	XP_011515236.1:p.Asp648_Leu656del
XM_011516935.1:c.1576_1602del	XP_011515237.1:p.Asp526_Leu534del
XM_011516936.1:c.1570_1596del	XP_011515238.1:p.Asp524_Leu532del
XM_011516937.1:c.1942_1968del	XP_011515239.1:p.Asp648_Leu656del
XM_011516938.1:c.1111_1137del	XP_011515240.1:p.Asp371_Leu379del
XM_011516939.1:c.640_666del	XP_011515241.1:p.Asp214_Leu222del
XM_011516940.1:c.640_666del	XP_011515242.1:p.Asp214_Leu222del
XM_011516941.1:c.1942_1968del	XP_011515243.1:p.Asp648_Leu656del
XM_011516942.1:c.1942_1968del	XP_011515244.1:p.Asp648_Leu656del
XR_242384.2:n.2072_2098del
XR_928310.1:n.2072_2098del
XR_928311.1:n.2072_2098del
XR_928312.1:n.2072_2098del
NM_001352890.2:c.2143_2169del	NP_001339819.2:p.Asp715_Leu723del
NM_001362798.1:c.2143_2169del	NP_001349727.1:p.Asp715_Leu723del
NM_014957.4:c.1942_1968del	NP_055772.3:p.Asp648_Leu656del
NR_148197.2:n.2239_2265del
XM_005250840.5:c.1987_2013del	XP_005250897.3:p.Asp663_Leu671del
XM_005250841.4:c.1987_2013del	XP_005250898.3:p.Asp663_Leu671del
XM_005250842.4:c.1909_1935del	XP_005250899.1:p.Asp637_Leu645del
XM_011516933.2:c.2143_2169del	XP_011515235.2:p.Asp715_Leu723del
XM_011516934.3:c.2143_2169del	XP_011515236.2:p.Asp715_Leu723del
XM_011516937.2:c.2143_2169del	XP_011515239.2:p.Asp715_Leu723del
XM_011516938.3:c.1111_1137del	XP_011515240.1:p.Asp371_Leu379del
XM_011516939.3:c.640_666del	XP_011515241.1:p.Asp214_Leu222del
XM_011516940.2:c.640_666del	XP_011515242.1:p.Asp214_Leu222del
XM_011516941.3:c.2143_2169del	XP_011515243.2:p.Asp715_Leu723del
XM_017013241.1:c.1942_1968del	XP_016868730.1:p.Asp648_Leu656del
XM_017013242.1:c.1399_1425del	XP_016868731.1:p.Asp467_Leu475del
XM_017013243.1:c.679_705del	XP_016868732.1:p.Asp227_Leu235del
XR_001745497.2:n.2289_2315del
XR_001745498.2:n.2289_2315del
XR_928310.3:n.2289_2315del
XR_928312.3:n.2289_2315del
NM_001352890.3:c.2143_2169del MANE Select	NP_001339819.2:p.Asp715_Leu723del
NM_001362798.2:c.2143_2169del	NP_001349727.1:p.Asp715_Leu723del
NM_014957.5:c.1942_1968del	NP_055772.3:p.Asp648_Leu656del
NR_148197.3:n.2262_2288del