Canonical Allele Identifier: CA473040242

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163585T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142038T>C , CM000673.2:g.9142038T>C	GRCh38
NC_000011.9:g.9163585T>C , CM000673.1:g.9163585T>C	GRCh37
NC_000011.8:g.9120161T>C	NCBI36
NG_053019.1:g.128298A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3582A>G MANE Select	ENSP00000328524.3:p.Arg1194=
ENST00000525784.6:n.1444A>G
ENST00000530780.2:c.*3408A>G	ENSP00000433925.1:n.*3408A>G
ENST00000531747.2:n.3253A>G
ENST00000679446.1:n.3503A>G
ENST00000679458.1:n.4983A>G
ENST00000679460.1:n.4644A>G
ENST00000679568.1:c.3582A>G	ENSP00000505860.1:p.Arg1194=
ENST00000679745.1:n.4087A>G
ENST00000679773.1:n.2743A>G
ENST00000679926.1:n.4884A>G
ENST00000679999.1:c.*639A>G	ENSP00000505198.1:n.*639A>G
ENST00000680252.1:c.3249A>G
ENST00000680294.1:c.3375A>G	ENSP00000506113.1:p.Arg1125=
ENST00000680358.1:n.2881A>G
ENST00000680470.1:c.*1363A>G	ENSP00000505975.1:n.*1363A>G
ENST00000680554.1:c.*115A>G	ENSP00000505621.1:n.*115A>G
ENST00000680576.1:n.5058A>G
ENST00000680599.1:n.3623A>G
ENST00000680742.1:c.*115A>G	ENSP00000505206.1:n.*115A>G
ENST00000680791.1:n.2466A>G
ENST00000680885.1:n.5284A>G
ENST00000681158.1:c.3166A>G
ENST00000681203.1:c.3510A>G	ENSP00000506456.1:p.Arg1170=
ENST00000681371.1:n.3454A>G
ENST00000681425.1:n.4060A>G
ENST00000681639.1:n.1861A>G
ENST00000328194.7:c.3582A>G	ENSP00000328524.3:p.Arg1194=
ENST00000525784.5:c.518A>G
ENST00000527700.5:n.3144A>G
ENST00000528725.5:c.278A>G
ENST00000529977.5:n.1483A>G
ENST00000530044.5:c.3582A>G	ENSP00000435866.1:p.Arg1194=
ENST00000531747.1:c.818A>G
ENST00000533737.5:c.245A>G
NM_001243254.1:c.3582A>G	NP_001230183.1:p.Arg1194=
NM_015213.3:c.3582A>G	NP_056028.2:p.Arg1194=
XM_005252832.1:c.3582A>G	XP_005252889.1:p.Arg1194=
XM_011519952.1:c.3582A>G	XP_011518254.1:p.Arg1194=
XM_011519953.1:c.1680A>G	XP_011518255.1:p.Arg560=
XR_242782.2:n.3764A>G
XR_930851.1:n.3764A>G
NM_001348749.1:c.3510A>G	NP_001335678.1:p.Arg1170=
NM_001348750.1:c.3294A>G	NP_001335679.1:p.Arg1098=
NR_145966.2:n.3756A>G
NM_015213.4:c.3582A>G MANE Select	NP_056028.2:p.Arg1194=
NM_001243254.2:c.3582A>G	NP_001230183.1:p.Arg1194=
NM_001348749.2:c.3510A>G	NP_001335678.1:p.Arg1170=
NM_001348750.2:c.3294A>G	NP_001335679.1:p.Arg1098=