Canonical Allele Identifier: CA372343631

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178181A>T (hg19) ; chr8:g.141168082A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168082A>T , CM000670.2:g.141168082A>T	GRCh38
NC_000008.10:g.142178181A>T , CM000670.1:g.142178181A>T	GRCh37
NC_000008.9:g.142247363A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1832A>T MANE Select	ENSP00000428714.1:p.Gln611Leu
ENST00000262585.6:c.1592A>T	ENSP00000262585.2:p.Gln531Leu
ENST00000424248.2:c.1436A>T	ENSP00000410594.1:p.Gln479Leu
ENST00000518668.5:c.1605A>T
ENST00000519811.5:c.1832A>T	ENSP00000428714.1:p.Gln611Leu
ENST00000520482.1:n.1373A>T
NM_014957.2:c.1592A>T	NP_055772.2:p.Gln531Leu
XM_005250838.3:c.1631A>T	XP_005250895.2:p.Gln544Leu
XM_005250839.2:c.1631A>T	XP_005250896.2:p.Gln544Leu
XM_005250840.3:c.1475A>T	XP_005250897.2:p.Gln492Leu
XM_005250841.2:c.1475A>T	XP_005250898.2:p.Gln492Leu
XM_005250842.3:c.1598A>T	XP_005250899.1:p.Gln533Leu
XM_005250843.3:c.1088A>T	XP_005250900.1:p.Gln363Leu
XM_011516933.1:c.1631A>T	XP_011515235.1:p.Gln544Leu
XM_011516934.1:c.1631A>T	XP_011515236.1:p.Gln544Leu
XM_011516935.1:c.1265A>T	XP_011515237.1:p.Gln422Leu
XM_011516936.1:c.1259A>T	XP_011515238.1:p.Gln420Leu
XM_011516937.1:c.1631A>T	XP_011515239.1:p.Gln544Leu
XM_011516938.1:c.800A>T	XP_011515240.1:p.Gln267Leu
XM_011516939.1:c.329A>T	XP_011515241.1:p.Gln110Leu
XM_011516940.1:c.329A>T	XP_011515242.1:p.Gln110Leu
XM_011516941.1:c.1631A>T	XP_011515243.1:p.Gln544Leu
XM_011516942.1:c.1631A>T	XP_011515244.1:p.Gln544Leu
XR_242384.2:n.1761A>T
XR_928310.1:n.1761A>T
XR_928311.1:n.1761A>T
XR_928312.1:n.1761A>T
NM_001352890.2:c.1832A>T	NP_001339819.2:p.Gln611Leu
NM_001362798.1:c.1832A>T	NP_001349727.1:p.Gln611Leu
NM_014957.4:c.1631A>T	NP_055772.3:p.Gln544Leu
NR_148197.2:n.1928A>T
XM_005250840.5:c.1676A>T	XP_005250897.3:p.Gln559Leu
XM_005250841.4:c.1676A>T	XP_005250898.3:p.Gln559Leu
XM_005250842.4:c.1598A>T	XP_005250899.1:p.Gln533Leu
XM_011516933.2:c.1832A>T	XP_011515235.2:p.Gln611Leu
XM_011516934.3:c.1832A>T	XP_011515236.2:p.Gln611Leu
XM_011516937.2:c.1832A>T	XP_011515239.2:p.Gln611Leu
XM_011516938.3:c.800A>T	XP_011515240.1:p.Gln267Leu
XM_011516939.3:c.329A>T	XP_011515241.1:p.Gln110Leu
XM_011516940.2:c.329A>T	XP_011515242.1:p.Gln110Leu
XM_011516941.3:c.1832A>T	XP_011515243.2:p.Gln611Leu
XM_017013241.1:c.1631A>T	XP_016868730.1:p.Gln544Leu
XM_017013242.1:c.1088A>T	XP_016868731.1:p.Gln363Leu
XM_017013243.1:c.368A>T	XP_016868732.1:p.Gln123Leu
XR_001745497.2:n.1978A>T
XR_001745498.2:n.1978A>T
XR_928310.3:n.1978A>T
XR_928312.3:n.1978A>T
NM_001352890.3:c.1832A>T MANE Select	NP_001339819.2:p.Gln611Leu
NM_001362798.2:c.1832A>T	NP_001349727.1:p.Gln611Leu
NM_014957.5:c.1631A>T	NP_055772.3:p.Gln544Leu
NR_148197.3:n.1951A>T