Canonical Allele Identifier: CA372344352

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178510T>C (hg19) ; chr8:g.141168411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168411T>C , CM000670.2:g.141168411T>C	GRCh38
NC_000008.10:g.142178510T>C , CM000670.1:g.142178510T>C	GRCh37
NC_000008.9:g.142247692T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2161T>C MANE Select	ENSP00000428714.1:p.Phe721Leu
ENST00000262585.6:c.1921T>C	ENSP00000262585.2:p.Phe641Leu
ENST00000424248.2:c.1765T>C	ENSP00000410594.1:p.Phe589Leu
ENST00000518668.5:c.1934T>C
ENST00000519811.5:c.2161T>C	ENSP00000428714.1:p.Phe721Leu
ENST00000520482.1:n.1702T>C
NM_014957.2:c.1921T>C	NP_055772.2:p.Phe641Leu
XM_005250838.3:c.1960T>C	XP_005250895.2:p.Phe654Leu
XM_005250839.2:c.1960T>C	XP_005250896.2:p.Phe654Leu
XM_005250840.3:c.1804T>C	XP_005250897.2:p.Phe602Leu
XM_005250841.2:c.1804T>C	XP_005250898.2:p.Phe602Leu
XM_005250842.3:c.1927T>C	XP_005250899.1:p.Phe643Leu
XM_005250843.3:c.1417T>C	XP_005250900.1:p.Phe473Leu
XM_011516933.1:c.1960T>C	XP_011515235.1:p.Phe654Leu
XM_011516934.1:c.1960T>C	XP_011515236.1:p.Phe654Leu
XM_011516935.1:c.1594T>C	XP_011515237.1:p.Phe532Leu
XM_011516936.1:c.1588T>C	XP_011515238.1:p.Phe530Leu
XM_011516937.1:c.1960T>C	XP_011515239.1:p.Phe654Leu
XM_011516938.1:c.1129T>C	XP_011515240.1:p.Phe377Leu
XM_011516939.1:c.658T>C	XP_011515241.1:p.Phe220Leu
XM_011516940.1:c.658T>C	XP_011515242.1:p.Phe220Leu
XM_011516941.1:c.1960T>C	XP_011515243.1:p.Phe654Leu
XM_011516942.1:c.1960T>C	XP_011515244.1:p.Phe654Leu
XR_242384.2:n.2090T>C
XR_928310.1:n.2090T>C
XR_928311.1:n.2090T>C
XR_928312.1:n.2090T>C
NM_001352890.2:c.2161T>C	NP_001339819.2:p.Phe721Leu
NM_001362798.1:c.2161T>C	NP_001349727.1:p.Phe721Leu
NM_014957.4:c.1960T>C	NP_055772.3:p.Phe654Leu
NR_148197.2:n.2257T>C
XM_005250840.5:c.2005T>C	XP_005250897.3:p.Phe669Leu
XM_005250841.4:c.2005T>C	XP_005250898.3:p.Phe669Leu
XM_005250842.4:c.1927T>C	XP_005250899.1:p.Phe643Leu
XM_011516933.2:c.2161T>C	XP_011515235.2:p.Phe721Leu
XM_011516934.3:c.2161T>C	XP_011515236.2:p.Phe721Leu
XM_011516937.2:c.2161T>C	XP_011515239.2:p.Phe721Leu
XM_011516938.3:c.1129T>C	XP_011515240.1:p.Phe377Leu
XM_011516939.3:c.658T>C	XP_011515241.1:p.Phe220Leu
XM_011516940.2:c.658T>C	XP_011515242.1:p.Phe220Leu
XM_011516941.3:c.2161T>C	XP_011515243.2:p.Phe721Leu
XM_017013241.1:c.1960T>C	XP_016868730.1:p.Phe654Leu
XM_017013242.1:c.1417T>C	XP_016868731.1:p.Phe473Leu
XM_017013243.1:c.697T>C	XP_016868732.1:p.Phe233Leu
XR_001745497.2:n.2307T>C
XR_001745498.2:n.2307T>C
XR_928310.3:n.2307T>C
XR_928312.3:n.2307T>C
NM_001352890.3:c.2161T>C MANE Select	NP_001339819.2:p.Phe721Leu
NM_001362798.2:c.2161T>C	NP_001349727.1:p.Phe721Leu
NM_014957.5:c.1960T>C	NP_055772.3:p.Phe654Leu
NR_148197.3:n.2280T>C