Canonical Allele Identifier: CA463493901

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178395C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168296C>A , CM000670.2:g.141168296C>A	GRCh38
NC_000008.10:g.142178395C>A , CM000670.1:g.142178395C>A	GRCh37
NC_000008.9:g.142247577C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2046C>A MANE Select	ENSP00000428714.1:p.Ser682=
ENST00000262585.6:c.1806C>A	ENSP00000262585.2:p.Ser602=
ENST00000424248.2:c.1650C>A	ENSP00000410594.1:p.Ser550=
ENST00000518668.5:c.1819C>A
ENST00000519811.5:c.2046C>A	ENSP00000428714.1:p.Ser682=
ENST00000520482.1:n.1587C>A
NM_014957.2:c.1806C>A	NP_055772.2:p.Ser602=
XM_005250838.3:c.1845C>A	XP_005250895.2:p.Ser615=
XM_005250839.2:c.1845C>A	XP_005250896.2:p.Ser615=
XM_005250840.3:c.1689C>A	XP_005250897.2:p.Ser563=
XM_005250841.2:c.1689C>A	XP_005250898.2:p.Ser563=
XM_005250842.3:c.1812C>A	XP_005250899.1:p.Ser604=
XM_005250843.3:c.1302C>A	XP_005250900.1:p.Ser434=
XM_011516933.1:c.1845C>A	XP_011515235.1:p.Ser615=
XM_011516934.1:c.1845C>A	XP_011515236.1:p.Ser615=
XM_011516935.1:c.1479C>A	XP_011515237.1:p.Ser493=
XM_011516936.1:c.1473C>A	XP_011515238.1:p.Ser491=
XM_011516937.1:c.1845C>A	XP_011515239.1:p.Ser615=
XM_011516938.1:c.1014C>A	XP_011515240.1:p.Ser338=
XM_011516939.1:c.543C>A	XP_011515241.1:p.Ser181=
XM_011516940.1:c.543C>A	XP_011515242.1:p.Ser181=
XM_011516941.1:c.1845C>A	XP_011515243.1:p.Ser615=
XM_011516942.1:c.1845C>A	XP_011515244.1:p.Ser615=
XR_242384.2:n.1975C>A
XR_928310.1:n.1975C>A
XR_928311.1:n.1975C>A
XR_928312.1:n.1975C>A
NM_001352890.2:c.2046C>A	NP_001339819.2:p.Ser682=
NM_001362798.1:c.2046C>A	NP_001349727.1:p.Ser682=
NM_014957.4:c.1845C>A	NP_055772.3:p.Ser615=
NR_148197.2:n.2142C>A
XM_005250840.5:c.1890C>A	XP_005250897.3:p.Ser630=
XM_005250841.4:c.1890C>A	XP_005250898.3:p.Ser630=
XM_005250842.4:c.1812C>A	XP_005250899.1:p.Ser604=
XM_011516933.2:c.2046C>A	XP_011515235.2:p.Ser682=
XM_011516934.3:c.2046C>A	XP_011515236.2:p.Ser682=
XM_011516937.2:c.2046C>A	XP_011515239.2:p.Ser682=
XM_011516938.3:c.1014C>A	XP_011515240.1:p.Ser338=
XM_011516939.3:c.543C>A	XP_011515241.1:p.Ser181=
XM_011516940.2:c.543C>A	XP_011515242.1:p.Ser181=
XM_011516941.3:c.2046C>A	XP_011515243.2:p.Ser682=
XM_017013241.1:c.1845C>A	XP_016868730.1:p.Ser615=
XM_017013242.1:c.1302C>A	XP_016868731.1:p.Ser434=
XM_017013243.1:c.582C>A	XP_016868732.1:p.Ser194=
XR_001745497.2:n.2192C>A
XR_001745498.2:n.2192C>A
XR_928310.3:n.2192C>A
XR_928312.3:n.2192C>A
NM_001352890.3:c.2046C>A MANE Select	NP_001339819.2:p.Ser682=
NM_001362798.2:c.2046C>A	NP_001349727.1:p.Ser682=
NM_014957.5:c.1845C>A	NP_055772.3:p.Ser615=
NR_148197.3:n.2165C>A