Canonical Allele Identifier: CA372344195

Gene: DENND3

Linked Data

• dbSNP Id: rs1411418482
• gnomAD v2: 8-142178441-A-G
• gnomAD v4: 8-141168342-A-G
• MyVariant Identifiers: chr8:g.142178441A>G (hg19) ; chr8:g.141168342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168342A>G , CM000670.2:g.141168342A>G	GRCh38
NC_000008.10:g.142178441A>G , CM000670.1:g.142178441A>G	GRCh37
NC_000008.9:g.142247623A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2092A>G MANE Select	ENSP00000428714.1:p.Met698Val
ENST00000262585.6:c.1852A>G	ENSP00000262585.2:p.Met618Val
ENST00000424248.2:c.1696A>G	ENSP00000410594.1:p.Met566Val
ENST00000518668.5:c.1865A>G
ENST00000519811.5:c.2092A>G	ENSP00000428714.1:p.Met698Val
ENST00000520482.1:n.1633A>G
NM_014957.2:c.1852A>G	NP_055772.2:p.Met618Val
XM_005250838.3:c.1891A>G	XP_005250895.2:p.Met631Val
XM_005250839.2:c.1891A>G	XP_005250896.2:p.Met631Val
XM_005250840.3:c.1735A>G	XP_005250897.2:p.Met579Val
XM_005250841.2:c.1735A>G	XP_005250898.2:p.Met579Val
XM_005250842.3:c.1858A>G	XP_005250899.1:p.Met620Val
XM_005250843.3:c.1348A>G	XP_005250900.1:p.Met450Val
XM_011516933.1:c.1891A>G	XP_011515235.1:p.Met631Val
XM_011516934.1:c.1891A>G	XP_011515236.1:p.Met631Val
XM_011516935.1:c.1525A>G	XP_011515237.1:p.Met509Val
XM_011516936.1:c.1519A>G	XP_011515238.1:p.Met507Val
XM_011516937.1:c.1891A>G	XP_011515239.1:p.Met631Val
XM_011516938.1:c.1060A>G	XP_011515240.1:p.Met354Val
XM_011516939.1:c.589A>G	XP_011515241.1:p.Met197Val
XM_011516940.1:c.589A>G	XP_011515242.1:p.Met197Val
XM_011516941.1:c.1891A>G	XP_011515243.1:p.Met631Val
XM_011516942.1:c.1891A>G	XP_011515244.1:p.Met631Val
XR_242384.2:n.2021A>G
XR_928310.1:n.2021A>G
XR_928311.1:n.2021A>G
XR_928312.1:n.2021A>G
NM_001352890.2:c.2092A>G	NP_001339819.2:p.Met698Val
NM_001362798.1:c.2092A>G	NP_001349727.1:p.Met698Val
NM_014957.4:c.1891A>G	NP_055772.3:p.Met631Val
NR_148197.2:n.2188A>G
XM_005250840.5:c.1936A>G	XP_005250897.3:p.Met646Val
XM_005250841.4:c.1936A>G	XP_005250898.3:p.Met646Val
XM_005250842.4:c.1858A>G	XP_005250899.1:p.Met620Val
XM_011516933.2:c.2092A>G	XP_011515235.2:p.Met698Val
XM_011516934.3:c.2092A>G	XP_011515236.2:p.Met698Val
XM_011516937.2:c.2092A>G	XP_011515239.2:p.Met698Val
XM_011516938.3:c.1060A>G	XP_011515240.1:p.Met354Val
XM_011516939.3:c.589A>G	XP_011515241.1:p.Met197Val
XM_011516940.2:c.589A>G	XP_011515242.1:p.Met197Val
XM_011516941.3:c.2092A>G	XP_011515243.2:p.Met698Val
XM_017013241.1:c.1891A>G	XP_016868730.1:p.Met631Val
XM_017013242.1:c.1348A>G	XP_016868731.1:p.Met450Val
XM_017013243.1:c.628A>G	XP_016868732.1:p.Met210Val
XR_001745497.2:n.2238A>G
XR_001745498.2:n.2238A>G
XR_928310.3:n.2238A>G
XR_928312.3:n.2238A>G
NM_001352890.3:c.2092A>G MANE Select	NP_001339819.2:p.Met698Val
NM_001362798.2:c.2092A>G	NP_001349727.1:p.Met698Val
NM_014957.5:c.1891A>G	NP_055772.3:p.Met631Val
NR_148197.3:n.2211A>G