Canonical Allele Identifier: CA652794005

Gene: DENND3

Linked Data

• COSMIC: COSN22804193

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168698_141168714del , CM000670.2:g.141168698_141168714del	GRCh38
NC_000008.10:g.142178797_142178813del , CM000670.1:g.142178797_142178813del	GRCh37
NC_000008.9:g.142247979_142247995del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2275+173_2275+189del MANE Select	ENSP00000428714.1:n.2275+173_2275+189del
ENST00000262585.6:c.2035+173_2035+189del	ENSP00000262585.2:n.2035+173_2035+189del
ENST00000424248.2:c.1879+173_1879+189del	ENSP00000410594.1:n.1879+173_1879+189del
ENST00000518668.5:c.2048+173_2048+189del
ENST00000519811.5:c.2275+173_2275+189del	ENSP00000428714.1:n.2275+173_2275+189del
ENST00000520482.1:n.1816+173_1816+189del
NM_014957.2:c.2035+173_2035+189del	NP_055772.2:n.2035+173_2035+189del
XM_005250838.3:c.2074+173_2074+189del	XP_005250895.2:n.2074+173_2074+189del
XM_005250839.2:c.2074+173_2074+189del	XP_005250896.2:n.2074+173_2074+189del
XM_005250840.3:c.1918+173_1918+189del	XP_005250897.2:n.1918+173_1918+189del
XM_005250841.2:c.1918+173_1918+189del	XP_005250898.2:n.1918+173_1918+189del
XM_005250842.3:c.2041+173_2041+189del	XP_005250899.1:n.2041+173_2041+189del
XM_005250843.3:c.1531+173_1531+189del	XP_005250900.1:n.1531+173_1531+189del
XM_011516933.1:c.2074+173_2074+189del	XP_011515235.1:n.2074+173_2074+189del
XM_011516934.1:c.2074+173_2074+189del	XP_011515236.1:n.2074+173_2074+189del
XM_011516935.1:c.1708+173_1708+189del	XP_011515237.1:n.1708+173_1708+189del
XM_011516936.1:c.1702+173_1702+189del	XP_011515238.1:n.1702+173_1702+189del
XM_011516937.1:c.2074+173_2074+189del	XP_011515239.1:n.2074+173_2074+189del
XM_011516938.1:c.1243+173_1243+189del	XP_011515240.1:n.1243+173_1243+189del
XM_011516939.1:c.772+173_772+189del	XP_011515241.1:n.772+173_772+189del
XM_011516940.1:c.772+173_772+189del	XP_011515242.1:n.772+173_772+189del
XM_011516941.1:c.2074+173_2074+189del	XP_011515243.1:n.2074+173_2074+189del
XM_011516942.1:c.2074+173_2074+189del	XP_011515244.1:n.2074+173_2074+189del
XR_242384.2:n.2204+173_2204+189del
XR_928310.1:n.2204+173_2204+189del
XR_928311.1:n.2204+173_2204+189del
XR_928312.1:n.2204+173_2204+189del
NM_001352890.2:c.2275+173_2275+189del	NP_001339819.2:n.2275+173_2275+189del
NM_001362798.1:c.2275+173_2275+189del	NP_001349727.1:n.2275+173_2275+189del
NM_014957.4:c.2074+173_2074+189del	NP_055772.3:n.2074+173_2074+189del
NR_148197.2:n.2371+173_2371+189del
XM_005250840.5:c.2119+173_2119+189del	XP_005250897.3:n.2119+173_2119+189del
XM_005250841.4:c.2119+173_2119+189del	XP_005250898.3:n.2119+173_2119+189del
XM_005250842.4:c.2041+173_2041+189del	XP_005250899.1:n.2041+173_2041+189del
XM_011516933.2:c.2275+173_2275+189del	XP_011515235.2:n.2275+173_2275+189del
XM_011516934.3:c.2275+173_2275+189del	XP_011515236.2:n.2275+173_2275+189del
XM_011516937.2:c.2275+173_2275+189del	XP_011515239.2:n.2275+173_2275+189del
XM_011516938.3:c.1243+173_1243+189del	XP_011515240.1:n.1243+173_1243+189del
XM_011516939.3:c.772+173_772+189del	XP_011515241.1:n.772+173_772+189del
XM_011516940.2:c.772+173_772+189del	XP_011515242.1:n.772+173_772+189del
XM_011516941.3:c.2275+173_2275+189del	XP_011515243.2:n.2275+173_2275+189del
XM_017013241.1:c.2074+173_2074+189del	XP_016868730.1:n.2074+173_2074+189del
XM_017013242.1:c.1531+173_1531+189del	XP_016868731.1:n.1531+173_1531+189del
XM_017013243.1:c.811+173_811+189del	XP_016868732.1:n.811+173_811+189del
XR_001745497.2:n.2421+173_2421+189del
XR_001745498.2:n.2421+173_2421+189del
XR_928310.3:n.2421+173_2421+189del
XR_928312.3:n.2421+173_2421+189del
NM_001352890.3:c.2275+173_2275+189del MANE Select	NP_001339819.2:n.2275+173_2275+189del
NM_001362798.2:c.2275+173_2275+189del	NP_001349727.1:n.2275+173_2275+189del
NM_014957.5:c.2074+173_2074+189del	NP_055772.3:n.2074+173_2074+189del
NR_148197.3:n.2394+173_2394+189del