Canonical Allele Identifier: CA463496997

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178512C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168413C>T , CM000670.2:g.141168413C>T	GRCh38
NC_000008.10:g.142178512C>T , CM000670.1:g.142178512C>T	GRCh37
NC_000008.9:g.142247694C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2163C>T MANE Select	ENSP00000428714.1:p.Phe721=
ENST00000262585.6:c.1923C>T	ENSP00000262585.2:p.Phe641=
ENST00000424248.2:c.1767C>T	ENSP00000410594.1:p.Phe589=
ENST00000518668.5:c.1936C>T
ENST00000519811.5:c.2163C>T	ENSP00000428714.1:p.Phe721=
ENST00000520482.1:n.1704C>T
NM_014957.2:c.1923C>T	NP_055772.2:p.Phe641=
XM_005250838.3:c.1962C>T	XP_005250895.2:p.Phe654=
XM_005250839.2:c.1962C>T	XP_005250896.2:p.Phe654=
XM_005250840.3:c.1806C>T	XP_005250897.2:p.Phe602=
XM_005250841.2:c.1806C>T	XP_005250898.2:p.Phe602=
XM_005250842.3:c.1929C>T	XP_005250899.1:p.Phe643=
XM_005250843.3:c.1419C>T	XP_005250900.1:p.Phe473=
XM_011516933.1:c.1962C>T	XP_011515235.1:p.Phe654=
XM_011516934.1:c.1962C>T	XP_011515236.1:p.Phe654=
XM_011516935.1:c.1596C>T	XP_011515237.1:p.Phe532=
XM_011516936.1:c.1590C>T	XP_011515238.1:p.Phe530=
XM_011516937.1:c.1962C>T	XP_011515239.1:p.Phe654=
XM_011516938.1:c.1131C>T	XP_011515240.1:p.Phe377=
XM_011516939.1:c.660C>T	XP_011515241.1:p.Phe220=
XM_011516940.1:c.660C>T	XP_011515242.1:p.Phe220=
XM_011516941.1:c.1962C>T	XP_011515243.1:p.Phe654=
XM_011516942.1:c.1962C>T	XP_011515244.1:p.Phe654=
XR_242384.2:n.2092C>T
XR_928310.1:n.2092C>T
XR_928311.1:n.2092C>T
XR_928312.1:n.2092C>T
NM_001352890.2:c.2163C>T	NP_001339819.2:p.Phe721=
NM_001362798.1:c.2163C>T	NP_001349727.1:p.Phe721=
NM_014957.4:c.1962C>T	NP_055772.3:p.Phe654=
NR_148197.2:n.2259C>T
XM_005250840.5:c.2007C>T	XP_005250897.3:p.Phe669=
XM_005250841.4:c.2007C>T	XP_005250898.3:p.Phe669=
XM_005250842.4:c.1929C>T	XP_005250899.1:p.Phe643=
XM_011516933.2:c.2163C>T	XP_011515235.2:p.Phe721=
XM_011516934.3:c.2163C>T	XP_011515236.2:p.Phe721=
XM_011516937.2:c.2163C>T	XP_011515239.2:p.Phe721=
XM_011516938.3:c.1131C>T	XP_011515240.1:p.Phe377=
XM_011516939.3:c.660C>T	XP_011515241.1:p.Phe220=
XM_011516940.2:c.660C>T	XP_011515242.1:p.Phe220=
XM_011516941.3:c.2163C>T	XP_011515243.2:p.Phe721=
XM_017013241.1:c.1962C>T	XP_016868730.1:p.Phe654=
XM_017013242.1:c.1419C>T	XP_016868731.1:p.Phe473=
XM_017013243.1:c.699C>T	XP_016868732.1:p.Phe233=
XR_001745497.2:n.2309C>T
XR_001745498.2:n.2309C>T
XR_928310.3:n.2309C>T
XR_928312.3:n.2309C>T
NM_001352890.3:c.2163C>T MANE Select	NP_001339819.2:p.Phe721=
NM_001362798.2:c.2163C>T	NP_001349727.1:p.Phe721=
NM_014957.5:c.1962C>T	NP_055772.3:p.Phe654=
NR_148197.3:n.2282C>T