Canonical Allele Identifier: CA2688780432

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168422-CAAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168426_141168428del , CM000670.2:g.141168426_141168428del	GRCh38
NC_000008.10:g.142178525_142178527del , CM000670.1:g.142178525_142178527del	GRCh37
NC_000008.9:g.142247707_142247709del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2176_2178del MANE Select	ENSP00000428714.1:p.Lys726del
ENST00000262585.6:c.1936_1938del	ENSP00000262585.2:p.Lys646del
ENST00000424248.2:c.1780_1782del	ENSP00000410594.1:p.Lys594del
ENST00000518668.5:c.1949_1951del
ENST00000519811.5:c.2176_2178del	ENSP00000428714.1:p.Lys726del
ENST00000520482.1:n.1717_1719del
NM_014957.2:c.1936_1938del	NP_055772.2:p.Lys646del
XM_005250838.3:c.1975_1977del	XP_005250895.2:p.Lys659del
XM_005250839.2:c.1975_1977del	XP_005250896.2:p.Lys659del
XM_005250840.3:c.1819_1821del	XP_005250897.2:p.Lys607del
XM_005250841.2:c.1819_1821del	XP_005250898.2:p.Lys607del
XM_005250842.3:c.1942_1944del	XP_005250899.1:p.Lys648del
XM_005250843.3:c.1432_1434del	XP_005250900.1:p.Lys478del
XM_011516933.1:c.1975_1977del	XP_011515235.1:p.Lys659del
XM_011516934.1:c.1975_1977del	XP_011515236.1:p.Lys659del
XM_011516935.1:c.1609_1611del	XP_011515237.1:p.Lys537del
XM_011516936.1:c.1603_1605del	XP_011515238.1:p.Lys535del
XM_011516937.1:c.1975_1977del	XP_011515239.1:p.Lys659del
XM_011516938.1:c.1144_1146del	XP_011515240.1:p.Lys382del
XM_011516939.1:c.673_675del	XP_011515241.1:p.Lys225del
XM_011516940.1:c.673_675del	XP_011515242.1:p.Lys225del
XM_011516941.1:c.1975_1977del	XP_011515243.1:p.Lys659del
XM_011516942.1:c.1975_1977del	XP_011515244.1:p.Lys659del
XR_242384.2:n.2105_2107del
XR_928310.1:n.2105_2107del
XR_928311.1:n.2105_2107del
XR_928312.1:n.2105_2107del
NM_001352890.2:c.2176_2178del	NP_001339819.2:p.Lys726del
NM_001362798.1:c.2176_2178del	NP_001349727.1:p.Lys726del
NM_014957.4:c.1975_1977del	NP_055772.3:p.Lys659del
NR_148197.2:n.2272_2274del
XM_005250840.5:c.2020_2022del	XP_005250897.3:p.Lys674del
XM_005250841.4:c.2020_2022del	XP_005250898.3:p.Lys674del
XM_005250842.4:c.1942_1944del	XP_005250899.1:p.Lys648del
XM_011516933.2:c.2176_2178del	XP_011515235.2:p.Lys726del
XM_011516934.3:c.2176_2178del	XP_011515236.2:p.Lys726del
XM_011516937.2:c.2176_2178del	XP_011515239.2:p.Lys726del
XM_011516938.3:c.1144_1146del	XP_011515240.1:p.Lys382del
XM_011516939.3:c.673_675del	XP_011515241.1:p.Lys225del
XM_011516940.2:c.673_675del	XP_011515242.1:p.Lys225del
XM_011516941.3:c.2176_2178del	XP_011515243.2:p.Lys726del
XM_017013241.1:c.1975_1977del	XP_016868730.1:p.Lys659del
XM_017013242.1:c.1432_1434del	XP_016868731.1:p.Lys478del
XM_017013243.1:c.712_714del	XP_016868732.1:p.Lys238del
XR_001745497.2:n.2322_2324del
XR_001745498.2:n.2322_2324del
XR_928310.3:n.2322_2324del
XR_928312.3:n.2322_2324del
NM_001352890.3:c.2176_2178del MANE Select	NP_001339819.2:p.Lys726del
NM_001362798.2:c.2176_2178del	NP_001349727.1:p.Lys726del
NM_014957.5:c.1975_1977del	NP_055772.3:p.Lys659del
NR_148197.3:n.2295_2297del