Canonical Allele Identifier: CA463493399

Gene: DENND3

Linked Data

• MyVariant Identifiers: chr8:g.142178278A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141168179A>C , CM000670.2:g.141168179A>C	GRCh38
NC_000008.10:g.142178278A>C , CM000670.1:g.142178278A>C	GRCh37
NC_000008.9:g.142247460A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519811.6:c.1929A>C MANE Select	ENSP00000428714.1:p.Arg643=
ENST00000262585.6:c.1689A>C	ENSP00000262585.2:p.Arg563=
ENST00000424248.2:c.1533A>C	ENSP00000410594.1:p.Arg511=
ENST00000518668.5:c.1702A>C
ENST00000519811.5:c.1929A>C	ENSP00000428714.1:p.Arg643=
ENST00000520482.1:n.1470A>C
NM_014957.2:c.1689A>C	NP_055772.2:p.Arg563=
XM_005250838.3:c.1728A>C	XP_005250895.2:p.Arg576=
XM_005250839.2:c.1728A>C	XP_005250896.2:p.Arg576=
XM_005250840.3:c.1572A>C	XP_005250897.2:p.Arg524=
XM_005250841.2:c.1572A>C	XP_005250898.2:p.Arg524=
XM_005250842.3:c.1695A>C	XP_005250899.1:p.Arg565=
XM_005250843.3:c.1185A>C	XP_005250900.1:p.Arg395=
XM_011516933.1:c.1728A>C	XP_011515235.1:p.Arg576=
XM_011516934.1:c.1728A>C	XP_011515236.1:p.Arg576=
XM_011516935.1:c.1362A>C	XP_011515237.1:p.Arg454=
XM_011516936.1:c.1356A>C	XP_011515238.1:p.Arg452=
XM_011516937.1:c.1728A>C	XP_011515239.1:p.Arg576=
XM_011516938.1:c.897A>C	XP_011515240.1:p.Arg299=
XM_011516939.1:c.426A>C	XP_011515241.1:p.Arg142=
XM_011516940.1:c.426A>C	XP_011515242.1:p.Arg142=
XM_011516941.1:c.1728A>C	XP_011515243.1:p.Arg576=
XM_011516942.1:c.1728A>C	XP_011515244.1:p.Arg576=
XR_242384.2:n.1858A>C
XR_928310.1:n.1858A>C
XR_928311.1:n.1858A>C
XR_928312.1:n.1858A>C
NM_001352890.2:c.1929A>C	NP_001339819.2:p.Arg643=
NM_001362798.1:c.1929A>C	NP_001349727.1:p.Arg643=
NM_014957.4:c.1728A>C	NP_055772.3:p.Arg576=
NR_148197.2:n.2025A>C
XM_005250840.5:c.1773A>C	XP_005250897.3:p.Arg591=
XM_005250841.4:c.1773A>C	XP_005250898.3:p.Arg591=
XM_005250842.4:c.1695A>C	XP_005250899.1:p.Arg565=
XM_011516933.2:c.1929A>C	XP_011515235.2:p.Arg643=
XM_011516934.3:c.1929A>C	XP_011515236.2:p.Arg643=
XM_011516937.2:c.1929A>C	XP_011515239.2:p.Arg643=
XM_011516938.3:c.897A>C	XP_011515240.1:p.Arg299=
XM_011516939.3:c.426A>C	XP_011515241.1:p.Arg142=
XM_011516940.2:c.426A>C	XP_011515242.1:p.Arg142=
XM_011516941.3:c.1929A>C	XP_011515243.2:p.Arg643=
XM_017013241.1:c.1728A>C	XP_016868730.1:p.Arg576=
XM_017013242.1:c.1185A>C	XP_016868731.1:p.Arg395=
XM_017013243.1:c.465A>C	XP_016868732.1:p.Arg155=
XR_001745497.2:n.2075A>C
XR_001745498.2:n.2075A>C
XR_928310.3:n.2075A>C
XR_928312.3:n.2075A>C
NM_001352890.3:c.1929A>C MANE Select	NP_001339819.2:p.Arg643=
NM_001362798.2:c.1929A>C	NP_001349727.1:p.Arg643=
NM_014957.5:c.1728A>C	NP_055772.3:p.Arg576=
NR_148197.3:n.2048A>C