Canonical Allele Identifier: CA2688780437

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168428-GCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168431_141168432del , CM000670.2:g.141168431_141168432del	GRCh38
NC_000008.10:g.142178530_142178531del , CM000670.1:g.142178530_142178531del	GRCh37
NC_000008.9:g.142247712_142247713del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2181_2182del MANE Select	ENSP00000428714.1:p.Met728AlafsTer?
ENST00000262585.6:c.1941_1942del	ENSP00000262585.2:p.Met648AlafsTer?
ENST00000424248.2:c.1785_1786del	ENSP00000410594.1:p.Met596AlafsTer?
ENST00000518668.5:c.1954_1955del
ENST00000519811.5:c.2181_2182del	ENSP00000428714.1:p.Met728AlafsTer?
ENST00000520482.1:n.1722_1723del
NM_014957.2:c.1941_1942del	NP_055772.2:p.Met648AlafsTer?
XM_005250838.3:c.1980_1981del	XP_005250895.2:p.Met661AlafsTer?
XM_005250839.2:c.1980_1981del	XP_005250896.2:p.Met661AlafsTer?
XM_005250840.3:c.1824_1825del	XP_005250897.2:p.Met609AlafsTer?
XM_005250841.2:c.1824_1825del	XP_005250898.2:p.Met609AlafsTer?
XM_005250842.3:c.1947_1948del	XP_005250899.1:p.Met650AlafsTer?
XM_005250843.3:c.1437_1438del	XP_005250900.1:p.Met480AlafsTer?
XM_011516933.1:c.1980_1981del	XP_011515235.1:p.Met661AlafsTer?
XM_011516934.1:c.1980_1981del	XP_011515236.1:p.Met661AlafsTer?
XM_011516935.1:c.1614_1615del	XP_011515237.1:p.Met539AlafsTer?
XM_011516936.1:c.1608_1609del	XP_011515238.1:p.Met537AlafsTer?
XM_011516937.1:c.1980_1981del	XP_011515239.1:p.Met661AlafsTer?
XM_011516938.1:c.1149_1150del	XP_011515240.1:p.Met384AlafsTer?
XM_011516939.1:c.678_679del	XP_011515241.1:p.Met227AlafsTer?
XM_011516940.1:c.678_679del	XP_011515242.1:p.Met227AlafsTer?
XM_011516941.1:c.1980_1981del	XP_011515243.1:p.Met661AlafsTer?
XM_011516942.1:c.1980_1981del	XP_011515244.1:p.Met661AlafsTer?
XR_242384.2:n.2110_2111del
XR_928310.1:n.2110_2111del
XR_928311.1:n.2110_2111del
XR_928312.1:n.2110_2111del
NM_001352890.2:c.2181_2182del	NP_001339819.2:p.Met728AlafsTer?
NM_001362798.1:c.2181_2182del	NP_001349727.1:p.Met728AlafsTer?
NM_014957.4:c.1980_1981del	NP_055772.3:p.Met661AlafsTer?
NR_148197.2:n.2277_2278del
XM_005250840.5:c.2025_2026del	XP_005250897.3:p.Met676AlafsTer?
XM_005250841.4:c.2025_2026del	XP_005250898.3:p.Met676AlafsTer?
XM_005250842.4:c.1947_1948del	XP_005250899.1:p.Met650AlafsTer?
XM_011516933.2:c.2181_2182del	XP_011515235.2:p.Met728AlafsTer?
XM_011516934.3:c.2181_2182del	XP_011515236.2:p.Met728AlafsTer?
XM_011516937.2:c.2181_2182del	XP_011515239.2:p.Met728AlafsTer?
XM_011516938.3:c.1149_1150del	XP_011515240.1:p.Met384AlafsTer?
XM_011516939.3:c.678_679del	XP_011515241.1:p.Met227AlafsTer?
XM_011516940.2:c.678_679del	XP_011515242.1:p.Met227AlafsTer?
XM_011516941.3:c.2181_2182del	XP_011515243.2:p.Met728AlafsTer?
XM_017013241.1:c.1980_1981del	XP_016868730.1:p.Met661AlafsTer?
XM_017013242.1:c.1437_1438del	XP_016868731.1:p.Met480AlafsTer?
XM_017013243.1:c.717_718del	XP_016868732.1:p.Met240AlafsTer?
XR_001745497.2:n.2327_2328del
XR_001745498.2:n.2327_2328del
XR_928310.3:n.2327_2328del
XR_928312.3:n.2327_2328del
NM_001352890.3:c.2181_2182del MANE Select	NP_001339819.2:p.Met728AlafsTer?
NM_001362798.2:c.2181_2182del	NP_001349727.1:p.Met728AlafsTer?
NM_014957.5:c.1980_1981del	NP_055772.3:p.Met661AlafsTer?
NR_148197.3:n.2300_2301del