Canonical Allele Identifier: CA372344099

Gene: DENND3

Linked Data

• gnomAD v4: 8-141168298-T-C
• MyVariant Identifiers: chr8:g.142178397T>C (hg19) ; chr8:g.141168298T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168298T>C , CM000670.2:g.141168298T>C	GRCh38
NC_000008.10:g.142178397T>C , CM000670.1:g.142178397T>C	GRCh37
NC_000008.9:g.142247579T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2048T>C MANE Select	ENSP00000428714.1:p.Met683Thr
ENST00000262585.6:c.1808T>C	ENSP00000262585.2:p.Met603Thr
ENST00000424248.2:c.1652T>C	ENSP00000410594.1:p.Met551Thr
ENST00000518668.5:c.1821T>C
ENST00000519811.5:c.2048T>C	ENSP00000428714.1:p.Met683Thr
ENST00000520482.1:n.1589T>C
NM_014957.2:c.1808T>C	NP_055772.2:p.Met603Thr
XM_005250838.3:c.1847T>C	XP_005250895.2:p.Met616Thr
XM_005250839.2:c.1847T>C	XP_005250896.2:p.Met616Thr
XM_005250840.3:c.1691T>C	XP_005250897.2:p.Met564Thr
XM_005250841.2:c.1691T>C	XP_005250898.2:p.Met564Thr
XM_005250842.3:c.1814T>C	XP_005250899.1:p.Met605Thr
XM_005250843.3:c.1304T>C	XP_005250900.1:p.Met435Thr
XM_011516933.1:c.1847T>C	XP_011515235.1:p.Met616Thr
XM_011516934.1:c.1847T>C	XP_011515236.1:p.Met616Thr
XM_011516935.1:c.1481T>C	XP_011515237.1:p.Met494Thr
XM_011516936.1:c.1475T>C	XP_011515238.1:p.Met492Thr
XM_011516937.1:c.1847T>C	XP_011515239.1:p.Met616Thr
XM_011516938.1:c.1016T>C	XP_011515240.1:p.Met339Thr
XM_011516939.1:c.545T>C	XP_011515241.1:p.Met182Thr
XM_011516940.1:c.545T>C	XP_011515242.1:p.Met182Thr
XM_011516941.1:c.1847T>C	XP_011515243.1:p.Met616Thr
XM_011516942.1:c.1847T>C	XP_011515244.1:p.Met616Thr
XR_242384.2:n.1977T>C
XR_928310.1:n.1977T>C
XR_928311.1:n.1977T>C
XR_928312.1:n.1977T>C
NM_001352890.2:c.2048T>C	NP_001339819.2:p.Met683Thr
NM_001362798.1:c.2048T>C	NP_001349727.1:p.Met683Thr
NM_014957.4:c.1847T>C	NP_055772.3:p.Met616Thr
NR_148197.2:n.2144T>C
XM_005250840.5:c.1892T>C	XP_005250897.3:p.Met631Thr
XM_005250841.4:c.1892T>C	XP_005250898.3:p.Met631Thr
XM_005250842.4:c.1814T>C	XP_005250899.1:p.Met605Thr
XM_011516933.2:c.2048T>C	XP_011515235.2:p.Met683Thr
XM_011516934.3:c.2048T>C	XP_011515236.2:p.Met683Thr
XM_011516937.2:c.2048T>C	XP_011515239.2:p.Met683Thr
XM_011516938.3:c.1016T>C	XP_011515240.1:p.Met339Thr
XM_011516939.3:c.545T>C	XP_011515241.1:p.Met182Thr
XM_011516940.2:c.545T>C	XP_011515242.1:p.Met182Thr
XM_011516941.3:c.2048T>C	XP_011515243.2:p.Met683Thr
XM_017013241.1:c.1847T>C	XP_016868730.1:p.Met616Thr
XM_017013242.1:c.1304T>C	XP_016868731.1:p.Met435Thr
XM_017013243.1:c.584T>C	XP_016868732.1:p.Met195Thr
XR_001745497.2:n.2194T>C
XR_001745498.2:n.2194T>C
XR_928310.3:n.2194T>C
XR_928312.3:n.2194T>C
NM_001352890.3:c.2048T>C MANE Select	NP_001339819.2:p.Met683Thr
NM_001362798.2:c.2048T>C	NP_001349727.1:p.Met683Thr
NM_014957.5:c.1847T>C	NP_055772.3:p.Met616Thr
NR_148197.3:n.2167T>C