Canonical Allele Identifier: CA372344029

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178364C>G (hg19) ; chr8:g.141168265C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168265C>G , CM000670.2:g.141168265C>G	GRCh38
NC_000008.10:g.142178364C>G , CM000670.1:g.142178364C>G	GRCh37
NC_000008.9:g.142247546C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.2015C>G MANE Select	ENSP00000428714.1:p.Pro672Arg
ENST00000262585.6:c.1775C>G	ENSP00000262585.2:p.Pro592Arg
ENST00000424248.2:c.1619C>G	ENSP00000410594.1:p.Pro540Arg
ENST00000518668.5:c.1788C>G
ENST00000519811.5:c.2015C>G	ENSP00000428714.1:p.Pro672Arg
ENST00000520482.1:n.1556C>G
NM_014957.2:c.1775C>G	NP_055772.2:p.Pro592Arg
XM_005250838.3:c.1814C>G	XP_005250895.2:p.Pro605Arg
XM_005250839.2:c.1814C>G	XP_005250896.2:p.Pro605Arg
XM_005250840.3:c.1658C>G	XP_005250897.2:p.Pro553Arg
XM_005250841.2:c.1658C>G	XP_005250898.2:p.Pro553Arg
XM_005250842.3:c.1781C>G	XP_005250899.1:p.Pro594Arg
XM_005250843.3:c.1271C>G	XP_005250900.1:p.Pro424Arg
XM_011516933.1:c.1814C>G	XP_011515235.1:p.Pro605Arg
XM_011516934.1:c.1814C>G	XP_011515236.1:p.Pro605Arg
XM_011516935.1:c.1448C>G	XP_011515237.1:p.Pro483Arg
XM_011516936.1:c.1442C>G	XP_011515238.1:p.Pro481Arg
XM_011516937.1:c.1814C>G	XP_011515239.1:p.Pro605Arg
XM_011516938.1:c.983C>G	XP_011515240.1:p.Pro328Arg
XM_011516939.1:c.512C>G	XP_011515241.1:p.Pro171Arg
XM_011516940.1:c.512C>G	XP_011515242.1:p.Pro171Arg
XM_011516941.1:c.1814C>G	XP_011515243.1:p.Pro605Arg
XM_011516942.1:c.1814C>G	XP_011515244.1:p.Pro605Arg
XR_242384.2:n.1944C>G
XR_928310.1:n.1944C>G
XR_928311.1:n.1944C>G
XR_928312.1:n.1944C>G
NM_001352890.2:c.2015C>G	NP_001339819.2:p.Pro672Arg
NM_001362798.1:c.2015C>G	NP_001349727.1:p.Pro672Arg
NM_014957.4:c.1814C>G	NP_055772.3:p.Pro605Arg
NR_148197.2:n.2111C>G
XM_005250840.5:c.1859C>G	XP_005250897.3:p.Pro620Arg
XM_005250841.4:c.1859C>G	XP_005250898.3:p.Pro620Arg
XM_005250842.4:c.1781C>G	XP_005250899.1:p.Pro594Arg
XM_011516933.2:c.2015C>G	XP_011515235.2:p.Pro672Arg
XM_011516934.3:c.2015C>G	XP_011515236.2:p.Pro672Arg
XM_011516937.2:c.2015C>G	XP_011515239.2:p.Pro672Arg
XM_011516938.3:c.983C>G	XP_011515240.1:p.Pro328Arg
XM_011516939.3:c.512C>G	XP_011515241.1:p.Pro171Arg
XM_011516940.2:c.512C>G	XP_011515242.1:p.Pro171Arg
XM_011516941.3:c.2015C>G	XP_011515243.2:p.Pro672Arg
XM_017013241.1:c.1814C>G	XP_016868730.1:p.Pro605Arg
XM_017013242.1:c.1271C>G	XP_016868731.1:p.Pro424Arg
XM_017013243.1:c.551C>G	XP_016868732.1:p.Pro184Arg
XR_001745497.2:n.2161C>G
XR_001745498.2:n.2161C>G
XR_928310.3:n.2161C>G
XR_928312.3:n.2161C>G
NM_001352890.3:c.2015C>G MANE Select	NP_001339819.2:p.Pro672Arg
NM_001362798.2:c.2015C>G	NP_001349727.1:p.Pro672Arg
NM_014957.5:c.1814C>G	NP_055772.3:p.Pro605Arg
NR_148197.3:n.2134C>G