Canonical Allele Identifier: CA372344151

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178420G>T (hg19) ; chr8:g.141168321G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168321G>T , CM000670.2:g.141168321G>T	GRCh38
NC_000008.10:g.142178420G>T , CM000670.1:g.142178420G>T	GRCh37
NC_000008.9:g.142247602G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000519811.6:c.2071G>T MANE Select	ENSP00000428714.1:p.Ala691Ser
ENST00000262585.6:c.1831G>T	ENSP00000262585.2:p.Ala611Ser
ENST00000424248.2:c.1675G>T	ENSP00000410594.1:p.Ala559Ser
ENST00000518668.5:c.1844G>T
ENST00000519811.5:c.2071G>T	ENSP00000428714.1:p.Ala691Ser
ENST00000520482.1:n.1612G>T
NM_014957.2:c.1831G>T	NP_055772.2:p.Ala611Ser
XM_005250838.3:c.1870G>T	XP_005250895.2:p.Ala624Ser
XM_005250839.2:c.1870G>T	XP_005250896.2:p.Ala624Ser
XM_005250840.3:c.1714G>T	XP_005250897.2:p.Ala572Ser
XM_005250841.2:c.1714G>T	XP_005250898.2:p.Ala572Ser
XM_005250842.3:c.1837G>T	XP_005250899.1:p.Ala613Ser
XM_005250843.3:c.1327G>T	XP_005250900.1:p.Ala443Ser
XM_011516933.1:c.1870G>T	XP_011515235.1:p.Ala624Ser
XM_011516934.1:c.1870G>T	XP_011515236.1:p.Ala624Ser
XM_011516935.1:c.1504G>T	XP_011515237.1:p.Ala502Ser
XM_011516936.1:c.1498G>T	XP_011515238.1:p.Ala500Ser
XM_011516937.1:c.1870G>T	XP_011515239.1:p.Ala624Ser
XM_011516938.1:c.1039G>T	XP_011515240.1:p.Ala347Ser
XM_011516939.1:c.568G>T	XP_011515241.1:p.Ala190Ser
XM_011516940.1:c.568G>T	XP_011515242.1:p.Ala190Ser
XM_011516941.1:c.1870G>T	XP_011515243.1:p.Ala624Ser
XM_011516942.1:c.1870G>T	XP_011515244.1:p.Ala624Ser
XR_242384.2:n.2000G>T
XR_928310.1:n.2000G>T
XR_928311.1:n.2000G>T
XR_928312.1:n.2000G>T
NM_001352890.2:c.2071G>T	NP_001339819.2:p.Ala691Ser
NM_001362798.1:c.2071G>T	NP_001349727.1:p.Ala691Ser
NM_014957.4:c.1870G>T	NP_055772.3:p.Ala624Ser
NR_148197.2:n.2167G>T
XM_005250840.5:c.1915G>T	XP_005250897.3:p.Ala639Ser
XM_005250841.4:c.1915G>T	XP_005250898.3:p.Ala639Ser
XM_005250842.4:c.1837G>T	XP_005250899.1:p.Ala613Ser
XM_011516933.2:c.2071G>T	XP_011515235.2:p.Ala691Ser
XM_011516934.3:c.2071G>T	XP_011515236.2:p.Ala691Ser
XM_011516937.2:c.2071G>T	XP_011515239.2:p.Ala691Ser
XM_011516938.3:c.1039G>T	XP_011515240.1:p.Ala347Ser
XM_011516939.3:c.568G>T	XP_011515241.1:p.Ala190Ser
XM_011516940.2:c.568G>T	XP_011515242.1:p.Ala190Ser
XM_011516941.3:c.2071G>T	XP_011515243.2:p.Ala691Ser
XM_017013241.1:c.1870G>T	XP_016868730.1:p.Ala624Ser
XM_017013242.1:c.1327G>T	XP_016868731.1:p.Ala443Ser
XM_017013243.1:c.607G>T	XP_016868732.1:p.Ala203Ser
XR_001745497.2:n.2217G>T
XR_001745498.2:n.2217G>T
XR_928310.3:n.2217G>T
XR_928312.3:n.2217G>T
NM_001352890.3:c.2071G>T MANE Select	NP_001339819.2:p.Ala691Ser
NM_001362798.2:c.2071G>T	NP_001349727.1:p.Ala691Ser
NM_014957.5:c.1870G>T	NP_055772.3:p.Ala624Ser
NR_148197.3:n.2190G>T