Canonical Allele Identifier: CA2688780327

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168316-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168321del , CM000670.2:g.141168321del	GRCh38
NC_000008.10:g.142178420del , CM000670.1:g.142178420del	GRCh37
NC_000008.9:g.142247602del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2071del MANE Select	ENSP00000428714.1:p.Ala691LeufsTer7
ENST00000262585.6:c.1831del	ENSP00000262585.2:p.Ala611LeufsTer7
ENST00000424248.2:c.1675del	ENSP00000410594.1:p.Ala559LeufsTer7
ENST00000518668.5:c.1844del
ENST00000519811.5:c.2071del	ENSP00000428714.1:p.Ala691LeufsTer7
ENST00000520482.1:n.1612del
NM_014957.2:c.1831del	NP_055772.2:p.Ala611LeufsTer7
XM_005250838.3:c.1870del	XP_005250895.2:p.Ala624LeufsTer7
XM_005250839.2:c.1870del	XP_005250896.2:p.Ala624LeufsTer7
XM_005250840.3:c.1714del	XP_005250897.2:p.Ala572LeufsTer7
XM_005250841.2:c.1714del	XP_005250898.2:p.Ala572LeufsTer7
XM_005250842.3:c.1837del	XP_005250899.1:p.Ala613LeufsTer7
XM_005250843.3:c.1327del	XP_005250900.1:p.Ala443LeufsTer7
XM_011516933.1:c.1870del	XP_011515235.1:p.Ala624LeufsTer7
XM_011516934.1:c.1870del	XP_011515236.1:p.Ala624LeufsTer7
XM_011516935.1:c.1504del	XP_011515237.1:p.Ala502LeufsTer7
XM_011516936.1:c.1498del	XP_011515238.1:p.Ala500LeufsTer7
XM_011516937.1:c.1870del	XP_011515239.1:p.Ala624LeufsTer7
XM_011516938.1:c.1039del	XP_011515240.1:p.Ala347LeufsTer7
XM_011516939.1:c.568del	XP_011515241.1:p.Ala190LeufsTer7
XM_011516940.1:c.568del	XP_011515242.1:p.Ala190LeufsTer7
XM_011516941.1:c.1870del	XP_011515243.1:p.Ala624LeufsTer7
XM_011516942.1:c.1870del	XP_011515244.1:p.Ala624LeufsTer7
XR_242384.2:n.2000del
XR_928310.1:n.2000del
XR_928311.1:n.2000del
XR_928312.1:n.2000del
NM_001352890.2:c.2071del	NP_001339819.2:p.Ala691LeufsTer7
NM_001362798.1:c.2071del	NP_001349727.1:p.Ala691LeufsTer7
NM_014957.4:c.1870del	NP_055772.3:p.Ala624LeufsTer7
NR_148197.2:n.2167del
XM_005250840.5:c.1915del	XP_005250897.3:p.Ala639LeufsTer7
XM_005250841.4:c.1915del	XP_005250898.3:p.Ala639LeufsTer7
XM_005250842.4:c.1837del	XP_005250899.1:p.Ala613LeufsTer7
XM_011516933.2:c.2071del	XP_011515235.2:p.Ala691LeufsTer7
XM_011516934.3:c.2071del	XP_011515236.2:p.Ala691LeufsTer7
XM_011516937.2:c.2071del	XP_011515239.2:p.Ala691LeufsTer7
XM_011516938.3:c.1039del	XP_011515240.1:p.Ala347LeufsTer7
XM_011516939.3:c.568del	XP_011515241.1:p.Ala190LeufsTer7
XM_011516940.2:c.568del	XP_011515242.1:p.Ala190LeufsTer7
XM_011516941.3:c.2071del	XP_011515243.2:p.Ala691LeufsTer7
XM_017013241.1:c.1870del	XP_016868730.1:p.Ala624LeufsTer7
XM_017013242.1:c.1327del	XP_016868731.1:p.Ala443LeufsTer7
XM_017013243.1:c.607del	XP_016868732.1:p.Ala203LeufsTer7
XR_001745497.2:n.2217del
XR_001745498.2:n.2217del
XR_928310.3:n.2217del
XR_928312.3:n.2217del
NM_001352890.3:c.2071del MANE Select	NP_001339819.2:p.Ala691LeufsTer7
NM_001362798.2:c.2071del	NP_001349727.1:p.Ala691LeufsTer7
NM_014957.5:c.1870del	NP_055772.3:p.Ala624LeufsTer7
NR_148197.3:n.2190del