Canonical Allele Identifier: CA4896396

Gene: DENND3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141150965C>T , CM000670.2:g.141150965C>T	GRCh38
NC_000008.10:g.142161064C>T , CM000670.1:g.142161064C>T	GRCh37
NC_000008.9:g.142230246C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.855+12C>T MANE Select	ENSP00000428714.1:n.855+12C>T
ENST00000262585.6:c.615+12C>T	ENSP00000262585.2:n.615+12C>T
ENST00000424248.2:c.615+12C>T	ENSP00000410594.1:n.615+12C>T
ENST00000518668.5:c.784+12C>T
ENST00000519811.5:c.855+12C>T	ENSP00000428714.1:n.855+12C>T
ENST00000520986.5:c.621+12C>T	ENSP00000429780.1:n.621+12C>T
NM_014957.2:c.615+12C>T	NP_055772.2:n.615+12C>T
XM_005250838.3:c.654+12C>T	XP_005250895.2:n.654+12C>T
XM_005250839.2:c.654+12C>T	XP_005250896.2:n.654+12C>T
XM_005250840.3:c.654+12C>T	XP_005250897.2:n.654+12C>T
XM_005250841.2:c.654+12C>T	XP_005250898.2:n.654+12C>T
XM_005250842.3:c.621+12C>T	XP_005250899.1:n.621+12C>T
XM_005250843.3:c.111+12C>T	XP_005250900.1:n.111+12C>T
XM_011516933.1:c.654+12C>T	XP_011515235.1:n.654+12C>T
XM_011516934.1:c.654+12C>T	XP_011515236.1:n.654+12C>T
XM_011516935.1:c.288+12C>T	XP_011515237.1:n.288+12C>T
XM_011516936.1:c.502-4884C>T	XP_011515238.1:n.502-4884C>T
XM_011516937.1:c.654+12C>T	XP_011515239.1:n.654+12C>T
XM_011516941.1:c.654+12C>T	XP_011515243.1:n.654+12C>T
XM_011516942.1:c.654+12C>T	XP_011515244.1:n.654+12C>T
XR_242384.2:n.784+12C>T
XR_928310.1:n.784+12C>T
XR_928311.1:n.784+12C>T
XR_928312.1:n.784+12C>T
NM_001352890.2:c.855+12C>T	NP_001339819.2:n.855+12C>T
NM_001362798.1:c.855+12C>T	NP_001349727.1:n.855+12C>T
NM_014957.4:c.654+12C>T	NP_055772.3:n.654+12C>T
NR_148197.2:n.951+12C>T
XM_005250840.5:c.855+12C>T	XP_005250897.3:n.855+12C>T
XM_005250841.4:c.855+12C>T	XP_005250898.3:n.855+12C>T
XM_005250842.4:c.621+12C>T	XP_005250899.1:n.621+12C>T
XM_011516933.2:c.855+12C>T	XP_011515235.2:n.855+12C>T
XM_011516934.3:c.855+12C>T	XP_011515236.2:n.855+12C>T
XM_011516937.2:c.855+12C>T	XP_011515239.2:n.855+12C>T
XM_011516941.3:c.855+12C>T	XP_011515243.2:n.855+12C>T
XM_017013241.1:c.654+12C>T	XP_016868730.1:n.654+12C>T
XM_017013242.1:c.111+12C>T	XP_016868731.1:n.111+12C>T
XR_001745497.2:n.1001+12C>T
XR_001745498.2:n.1001+12C>T
XR_928310.3:n.1001+12C>T
XR_928312.3:n.1001+12C>T
NM_001352890.3:c.855+12C>T MANE Select	NP_001339819.2:n.855+12C>T
NM_001362798.2:c.855+12C>T	NP_001349727.1:n.855+12C>T
NM_014957.5:c.654+12C>T	NP_055772.3:n.654+12C>T
NR_148197.3:n.974+12C>T