Canonical Allele Identifier: CA463497005

Gene: DENND3

Linked Data

• COSMIC: COSM3319838
• MyVariant Identifiers: chr8:g.142178518G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168419G>A , CM000670.2:g.141168419G>A	GRCh38
NC_000008.10:g.142178518G>A , CM000670.1:g.142178518G>A	GRCh37
NC_000008.9:g.142247700G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2169G>A MANE Select	ENSP00000428714.1:p.Leu723=
ENST00000262585.6:c.1929G>A	ENSP00000262585.2:p.Leu643=
ENST00000424248.2:c.1773G>A	ENSP00000410594.1:p.Leu591=
ENST00000518668.5:c.1942G>A
ENST00000519811.5:c.2169G>A	ENSP00000428714.1:p.Leu723=
ENST00000520482.1:n.1710G>A
NM_014957.2:c.1929G>A	NP_055772.2:p.Leu643=
XM_005250838.3:c.1968G>A	XP_005250895.2:p.Leu656=
XM_005250839.2:c.1968G>A	XP_005250896.2:p.Leu656=
XM_005250840.3:c.1812G>A	XP_005250897.2:p.Leu604=
XM_005250841.2:c.1812G>A	XP_005250898.2:p.Leu604=
XM_005250842.3:c.1935G>A	XP_005250899.1:p.Leu645=
XM_005250843.3:c.1425G>A	XP_005250900.1:p.Leu475=
XM_011516933.1:c.1968G>A	XP_011515235.1:p.Leu656=
XM_011516934.1:c.1968G>A	XP_011515236.1:p.Leu656=
XM_011516935.1:c.1602G>A	XP_011515237.1:p.Leu534=
XM_011516936.1:c.1596G>A	XP_011515238.1:p.Leu532=
XM_011516937.1:c.1968G>A	XP_011515239.1:p.Leu656=
XM_011516938.1:c.1137G>A	XP_011515240.1:p.Leu379=
XM_011516939.1:c.666G>A	XP_011515241.1:p.Leu222=
XM_011516940.1:c.666G>A	XP_011515242.1:p.Leu222=
XM_011516941.1:c.1968G>A	XP_011515243.1:p.Leu656=
XM_011516942.1:c.1968G>A	XP_011515244.1:p.Leu656=
XR_242384.2:n.2098G>A
XR_928310.1:n.2098G>A
XR_928311.1:n.2098G>A
XR_928312.1:n.2098G>A
NM_001352890.2:c.2169G>A	NP_001339819.2:p.Leu723=
NM_001362798.1:c.2169G>A	NP_001349727.1:p.Leu723=
NM_014957.4:c.1968G>A	NP_055772.3:p.Leu656=
NR_148197.2:n.2265G>A
XM_005250840.5:c.2013G>A	XP_005250897.3:p.Leu671=
XM_005250841.4:c.2013G>A	XP_005250898.3:p.Leu671=
XM_005250842.4:c.1935G>A	XP_005250899.1:p.Leu645=
XM_011516933.2:c.2169G>A	XP_011515235.2:p.Leu723=
XM_011516934.3:c.2169G>A	XP_011515236.2:p.Leu723=
XM_011516937.2:c.2169G>A	XP_011515239.2:p.Leu723=
XM_011516938.3:c.1137G>A	XP_011515240.1:p.Leu379=
XM_011516939.3:c.666G>A	XP_011515241.1:p.Leu222=
XM_011516940.2:c.666G>A	XP_011515242.1:p.Leu222=
XM_011516941.3:c.2169G>A	XP_011515243.2:p.Leu723=
XM_017013241.1:c.1968G>A	XP_016868730.1:p.Leu656=
XM_017013242.1:c.1425G>A	XP_016868731.1:p.Leu475=
XM_017013243.1:c.705G>A	XP_016868732.1:p.Leu235=
XR_001745497.2:n.2315G>A
XR_001745498.2:n.2315G>A
XR_928310.3:n.2315G>A
XR_928312.3:n.2315G>A
NM_001352890.3:c.2169G>A MANE Select	NP_001339819.2:p.Leu723=
NM_001362798.2:c.2169G>A	NP_001349727.1:p.Leu723=
NM_014957.5:c.1968G>A	NP_055772.3:p.Leu656=
NR_148197.3:n.2288G>A