Canonical Allele Identifier: CA2550670887

Gene: DENND3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168309_141168310insTATCATTAAAAA , CM000670.2:g.141168309_141168310insTATCATTAAAAA	GRCh38
NC_000008.10:g.142178408_142178409insTATCATTAAAAA , CM000670.1:g.142178408_142178409insTATCATTAAAAA	GRCh37
NC_000008.9:g.142247590_142247591insTATCATTAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2059_2060insTATCATTAAAAA MANE Select	ENSP00000428714.1:p.Glu687delinsValSerLeuLysLys
ENST00000262585.6:c.1819_1820insTATCATTAAAAA	ENSP00000262585.2:p.Glu607delinsValSerLeuLysLys
ENST00000424248.2:c.1663_1664insTATCATTAAAAA	ENSP00000410594.1:p.Glu555delinsValSerLeuLysLys
ENST00000518668.5:c.1832_1833insTATCATTAAAAA
ENST00000519811.5:c.2059_2060insTATCATTAAAAA	ENSP00000428714.1:p.Glu687delinsValSerLeuLysLys
ENST00000520482.1:n.1600_1601insTATCATTAAAAA
NM_014957.2:c.1819_1820insTATCATTAAAAA	NP_055772.2:p.Glu607delinsValSerLeuLysLys
XM_005250838.3:c.1858_1859insTATCATTAAAAA	XP_005250895.2:p.Glu620delinsValSerLeuLysLys
XM_005250839.2:c.1858_1859insTATCATTAAAAA	XP_005250896.2:p.Glu620delinsValSerLeuLysLys
XM_005250840.3:c.1702_1703insTATCATTAAAAA	XP_005250897.2:p.Glu568delinsValSerLeuLysLys
XM_005250841.2:c.1702_1703insTATCATTAAAAA	XP_005250898.2:p.Glu568delinsValSerLeuLysLys
XM_005250842.3:c.1825_1826insTATCATTAAAAA	XP_005250899.1:p.Glu609delinsValSerLeuLysLys
XM_005250843.3:c.1315_1316insTATCATTAAAAA	XP_005250900.1:p.Glu439delinsValSerLeuLysLys
XM_011516933.1:c.1858_1859insTATCATTAAAAA	XP_011515235.1:p.Glu620delinsValSerLeuLysLys
XM_011516934.1:c.1858_1859insTATCATTAAAAA	XP_011515236.1:p.Glu620delinsValSerLeuLysLys
XM_011516935.1:c.1492_1493insTATCATTAAAAA	XP_011515237.1:p.Glu498delinsValSerLeuLysLys
XM_011516936.1:c.1486_1487insTATCATTAAAAA	XP_011515238.1:p.Glu496delinsValSerLeuLysLys
XM_011516937.1:c.1858_1859insTATCATTAAAAA	XP_011515239.1:p.Glu620delinsValSerLeuLysLys
XM_011516938.1:c.1027_1028insTATCATTAAAAA	XP_011515240.1:p.Glu343delinsValSerLeuLysLys
XM_011516939.1:c.556_557insTATCATTAAAAA	XP_011515241.1:p.Glu186delinsValSerLeuLysLys
XM_011516940.1:c.556_557insTATCATTAAAAA	XP_011515242.1:p.Glu186delinsValSerLeuLysLys
XM_011516941.1:c.1858_1859insTATCATTAAAAA	XP_011515243.1:p.Glu620delinsValSerLeuLysLys
XM_011516942.1:c.1858_1859insTATCATTAAAAA	XP_011515244.1:p.Glu620delinsValSerLeuLysLys
XR_242384.2:n.1988_1989insTATCATTAAAAA
XR_928310.1:n.1988_1989insTATCATTAAAAA
XR_928311.1:n.1988_1989insTATCATTAAAAA
XR_928312.1:n.1988_1989insTATCATTAAAAA
NM_001352890.2:c.2059_2060insTATCATTAAAAA	NP_001339819.2:p.Glu687delinsValSerLeuLysLys
NM_001362798.1:c.2059_2060insTATCATTAAAAA	NP_001349727.1:p.Glu687delinsValSerLeuLysLys
NM_014957.4:c.1858_1859insTATCATTAAAAA	NP_055772.3:p.Glu620delinsValSerLeuLysLys
NR_148197.2:n.2155_2156insTATCATTAAAAA
XM_005250840.5:c.1903_1904insTATCATTAAAAA	XP_005250897.3:p.Glu635delinsValSerLeuLysLys
XM_005250841.4:c.1903_1904insTATCATTAAAAA	XP_005250898.3:p.Glu635delinsValSerLeuLysLys
XM_005250842.4:c.1825_1826insTATCATTAAAAA	XP_005250899.1:p.Glu609delinsValSerLeuLysLys
XM_011516933.2:c.2059_2060insTATCATTAAAAA	XP_011515235.2:p.Glu687delinsValSerLeuLysLys
XM_011516934.3:c.2059_2060insTATCATTAAAAA	XP_011515236.2:p.Glu687delinsValSerLeuLysLys
XM_011516937.2:c.2059_2060insTATCATTAAAAA	XP_011515239.2:p.Glu687delinsValSerLeuLysLys
XM_011516938.3:c.1027_1028insTATCATTAAAAA	XP_011515240.1:p.Glu343delinsValSerLeuLysLys
XM_011516939.3:c.556_557insTATCATTAAAAA	XP_011515241.1:p.Glu186delinsValSerLeuLysLys
XM_011516940.2:c.556_557insTATCATTAAAAA	XP_011515242.1:p.Glu186delinsValSerLeuLysLys
XM_011516941.3:c.2059_2060insTATCATTAAAAA	XP_011515243.2:p.Glu687delinsValSerLeuLysLys
XM_017013241.1:c.1858_1859insTATCATTAAAAA	XP_016868730.1:p.Glu620delinsValSerLeuLysLys
XM_017013242.1:c.1315_1316insTATCATTAAAAA	XP_016868731.1:p.Glu439delinsValSerLeuLysLys
XM_017013243.1:c.595_596insTATCATTAAAAA	XP_016868732.1:p.Glu199delinsValSerLeuLysLys
XR_001745497.2:n.2205_2206insTATCATTAAAAA
XR_001745498.2:n.2205_2206insTATCATTAAAAA
XR_928310.3:n.2205_2206insTATCATTAAAAA
XR_928312.3:n.2205_2206insTATCATTAAAAA
NM_001352890.3:c.2059_2060insTATCATTAAAAA MANE Select	NP_001339819.2:p.Glu687delinsValSerLeuLysLys
NM_001362798.2:c.2059_2060insTATCATTAAAAA	NP_001349727.1:p.Glu687delinsValSerLeuLysLys
NM_014957.5:c.1858_1859insTATCATTAAAAA	NP_055772.3:p.Glu620delinsValSerLeuLysLys
NR_148197.3:n.2178_2179insTATCATTAAAAA