Canonical Allele Identifier: CA2528185892

Gene: DENND3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168296_141168302del , CM000670.2:g.141168296_141168302del	GRCh38
NC_000008.10:g.142178395_142178401del , CM000670.1:g.142178395_142178401del	GRCh37
NC_000008.9:g.142247577_142247583del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2046_2052del MANE Select	ENSP00000428714.1:p.Met683ProfsTer13
ENST00000262585.6:c.1806_1812del	ENSP00000262585.2:p.Met603ProfsTer13
ENST00000424248.2:c.1650_1656del	ENSP00000410594.1:p.Met551ProfsTer13
ENST00000518668.5:c.1819_1825del
ENST00000519811.5:c.2046_2052del	ENSP00000428714.1:p.Met683ProfsTer13
ENST00000520482.1:n.1587_1593del
NM_014957.2:c.1806_1812del	NP_055772.2:p.Met603ProfsTer13
XM_005250838.3:c.1845_1851del	XP_005250895.2:p.Met616ProfsTer13
XM_005250839.2:c.1845_1851del	XP_005250896.2:p.Met616ProfsTer13
XM_005250840.3:c.1689_1695del	XP_005250897.2:p.Met564ProfsTer13
XM_005250841.2:c.1689_1695del	XP_005250898.2:p.Met564ProfsTer13
XM_005250842.3:c.1812_1818del	XP_005250899.1:p.Met605ProfsTer13
XM_005250843.3:c.1302_1308del	XP_005250900.1:p.Met435ProfsTer13
XM_011516933.1:c.1845_1851del	XP_011515235.1:p.Met616ProfsTer13
XM_011516934.1:c.1845_1851del	XP_011515236.1:p.Met616ProfsTer13
XM_011516935.1:c.1479_1485del	XP_011515237.1:p.Met494ProfsTer13
XM_011516936.1:c.1473_1479del	XP_011515238.1:p.Met492ProfsTer13
XM_011516937.1:c.1845_1851del	XP_011515239.1:p.Met616ProfsTer13
XM_011516938.1:c.1014_1020del	XP_011515240.1:p.Met339ProfsTer13
XM_011516939.1:c.543_549del	XP_011515241.1:p.Met182ProfsTer13
XM_011516940.1:c.543_549del	XP_011515242.1:p.Met182ProfsTer13
XM_011516941.1:c.1845_1851del	XP_011515243.1:p.Met616ProfsTer13
XM_011516942.1:c.1845_1851del	XP_011515244.1:p.Met616ProfsTer13
XR_242384.2:n.1975_1981del
XR_928310.1:n.1975_1981del
XR_928311.1:n.1975_1981del
XR_928312.1:n.1975_1981del
NM_001352890.2:c.2046_2052del	NP_001339819.2:p.Met683ProfsTer13
NM_001362798.1:c.2046_2052del	NP_001349727.1:p.Met683ProfsTer13
NM_014957.4:c.1845_1851del	NP_055772.3:p.Met616ProfsTer13
NR_148197.2:n.2142_2148del
XM_005250840.5:c.1890_1896del	XP_005250897.3:p.Met631ProfsTer13
XM_005250841.4:c.1890_1896del	XP_005250898.3:p.Met631ProfsTer13
XM_005250842.4:c.1812_1818del	XP_005250899.1:p.Met605ProfsTer13
XM_011516933.2:c.2046_2052del	XP_011515235.2:p.Met683ProfsTer13
XM_011516934.3:c.2046_2052del	XP_011515236.2:p.Met683ProfsTer13
XM_011516937.2:c.2046_2052del	XP_011515239.2:p.Met683ProfsTer13
XM_011516938.3:c.1014_1020del	XP_011515240.1:p.Met339ProfsTer13
XM_011516939.3:c.543_549del	XP_011515241.1:p.Met182ProfsTer13
XM_011516940.2:c.543_549del	XP_011515242.1:p.Met182ProfsTer13
XM_011516941.3:c.2046_2052del	XP_011515243.2:p.Met683ProfsTer13
XM_017013241.1:c.1845_1851del	XP_016868730.1:p.Met616ProfsTer13
XM_017013242.1:c.1302_1308del	XP_016868731.1:p.Met435ProfsTer13
XM_017013243.1:c.582_588del	XP_016868732.1:p.Met195ProfsTer13
XR_001745497.2:n.2192_2198del
XR_001745498.2:n.2192_2198del
XR_928310.3:n.2192_2198del
XR_928312.3:n.2192_2198del
NM_001352890.3:c.2046_2052del MANE Select	NP_001339819.2:p.Met683ProfsTer13
NM_001362798.2:c.2046_2052del	NP_001349727.1:p.Met683ProfsTer13
NM_014957.5:c.1845_1851del	NP_055772.3:p.Met616ProfsTer13
NR_148197.3:n.2165_2171del