Canonical Allele Identifier: CA1119983421

Gene: DENND3

Linked Data

• dbSNP Id: rs1821119611
• gnomAD v3: 8-141168716-A-ATT
• gnomAD v4: 8-141168716-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168716_141168717insTT , CM000670.2:g.141168716_141168717insTT	GRCh38
NC_000008.10:g.142178815_142178816insTT , CM000670.1:g.142178815_142178816insTT	GRCh37
NC_000008.9:g.142247997_142247998insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2275+191_2275+192insTT MANE Select	ENSP00000428714.1:n.2275+191_2275+192insTT
ENST00000262585.6:c.2035+191_2035+192insTT	ENSP00000262585.2:n.2035+191_2035+192insTT
ENST00000424248.2:c.1879+191_1879+192insTT	ENSP00000410594.1:n.1879+191_1879+192insTT
ENST00000518668.5:c.2048+191_2048+192insTT
ENST00000519811.5:c.2275+191_2275+192insTT	ENSP00000428714.1:n.2275+191_2275+192insTT
ENST00000520482.1:n.1816+191_1816+192insTT
NM_014957.2:c.2035+191_2035+192insTT	NP_055772.2:n.2035+191_2035+192insTT
XM_005250838.3:c.2074+191_2074+192insTT	XP_005250895.2:n.2074+191_2074+192insTT
XM_005250839.2:c.2074+191_2074+192insTT	XP_005250896.2:n.2074+191_2074+192insTT
XM_005250840.3:c.1918+191_1918+192insTT	XP_005250897.2:n.1918+191_1918+192insTT
XM_005250841.2:c.1918+191_1918+192insTT	XP_005250898.2:n.1918+191_1918+192insTT
XM_005250842.3:c.2041+191_2041+192insTT	XP_005250899.1:n.2041+191_2041+192insTT
XM_005250843.3:c.1531+191_1531+192insTT	XP_005250900.1:n.1531+191_1531+192insTT
XM_011516933.1:c.2074+191_2074+192insTT	XP_011515235.1:n.2074+191_2074+192insTT
XM_011516934.1:c.2074+191_2074+192insTT	XP_011515236.1:n.2074+191_2074+192insTT
XM_011516935.1:c.1708+191_1708+192insTT	XP_011515237.1:n.1708+191_1708+192insTT
XM_011516936.1:c.1702+191_1702+192insTT	XP_011515238.1:n.1702+191_1702+192insTT
XM_011516937.1:c.2074+191_2074+192insTT	XP_011515239.1:n.2074+191_2074+192insTT
XM_011516938.1:c.1243+191_1243+192insTT	XP_011515240.1:n.1243+191_1243+192insTT
XM_011516939.1:c.772+191_772+192insTT	XP_011515241.1:n.772+191_772+192insTT
XM_011516940.1:c.772+191_772+192insTT	XP_011515242.1:n.772+191_772+192insTT
XM_011516941.1:c.2074+191_2074+192insTT	XP_011515243.1:n.2074+191_2074+192insTT
XM_011516942.1:c.2074+191_2074+192insTT	XP_011515244.1:n.2074+191_2074+192insTT
XR_242384.2:n.2204+191_2204+192insTT
XR_928310.1:n.2204+191_2204+192insTT
XR_928311.1:n.2204+191_2204+192insTT
XR_928312.1:n.2204+191_2204+192insTT
NM_001352890.2:c.2275+191_2275+192insTT	NP_001339819.2:n.2275+191_2275+192insTT
NM_001362798.1:c.2275+191_2275+192insTT	NP_001349727.1:n.2275+191_2275+192insTT
NM_014957.4:c.2074+191_2074+192insTT	NP_055772.3:n.2074+191_2074+192insTT
NR_148197.2:n.2371+191_2371+192insTT
XM_005250840.5:c.2119+191_2119+192insTT	XP_005250897.3:n.2119+191_2119+192insTT
XM_005250841.4:c.2119+191_2119+192insTT	XP_005250898.3:n.2119+191_2119+192insTT
XM_005250842.4:c.2041+191_2041+192insTT	XP_005250899.1:n.2041+191_2041+192insTT
XM_011516933.2:c.2275+191_2275+192insTT	XP_011515235.2:n.2275+191_2275+192insTT
XM_011516934.3:c.2275+191_2275+192insTT	XP_011515236.2:n.2275+191_2275+192insTT
XM_011516937.2:c.2275+191_2275+192insTT	XP_011515239.2:n.2275+191_2275+192insTT
XM_011516938.3:c.1243+191_1243+192insTT	XP_011515240.1:n.1243+191_1243+192insTT
XM_011516939.3:c.772+191_772+192insTT	XP_011515241.1:n.772+191_772+192insTT
XM_011516940.2:c.772+191_772+192insTT	XP_011515242.1:n.772+191_772+192insTT
XM_011516941.3:c.2275+191_2275+192insTT	XP_011515243.2:n.2275+191_2275+192insTT
XM_017013241.1:c.2074+191_2074+192insTT	XP_016868730.1:n.2074+191_2074+192insTT
XM_017013242.1:c.1531+191_1531+192insTT	XP_016868731.1:n.1531+191_1531+192insTT
XM_017013243.1:c.811+191_811+192insTT	XP_016868732.1:n.811+191_811+192insTT
XR_001745497.2:n.2421+191_2421+192insTT
XR_001745498.2:n.2421+191_2421+192insTT
XR_928310.3:n.2421+191_2421+192insTT
XR_928312.3:n.2421+191_2421+192insTT
NM_001352890.3:c.2275+191_2275+192insTT MANE Select	NP_001339819.2:n.2275+191_2275+192insTT
NM_001362798.2:c.2275+191_2275+192insTT	NP_001349727.1:n.2275+191_2275+192insTT
NM_014957.5:c.2074+191_2074+192insTT	NP_055772.3:n.2074+191_2074+192insTT
NR_148197.3:n.2394+191_2394+192insTT