Canonical Allele Identifier: CA473040183

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163492T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141945T>A , CM000673.2:g.9141945T>A	GRCh38
NC_000011.9:g.9163492T>A , CM000673.1:g.9163492T>A	GRCh37
NC_000011.8:g.9120068T>A	NCBI36
NG_053019.1:g.128391A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3675A>T MANE Select	ENSP00000328524.3:p.Gly1225=
ENST00000525784.6:n.1537A>T
ENST00000530780.2:c.*3501A>T	ENSP00000433925.1:n.*3501A>T
ENST00000531747.2:n.3346A>T
ENST00000679446.1:n.3596A>T
ENST00000679458.1:n.5076A>T
ENST00000679460.1:n.4737A>T
ENST00000679568.1:c.3675A>T	ENSP00000505860.1:p.Gly1225=
ENST00000679745.1:n.4180A>T
ENST00000679773.1:n.2836A>T
ENST00000679926.1:n.4977A>T
ENST00000679999.1:c.*732A>T	ENSP00000505198.1:n.*732A>T
ENST00000680252.1:c.3342A>T
ENST00000680294.1:c.3468A>T	ENSP00000506113.1:p.Gly1156=
ENST00000680358.1:n.2974A>T
ENST00000680470.1:c.*1456A>T	ENSP00000505975.1:n.*1456A>T
ENST00000680554.1:c.*208A>T	ENSP00000505621.1:n.*208A>T
ENST00000680576.1:n.5151A>T
ENST00000680599.1:n.3716A>T
ENST00000680742.1:c.*179+29A>T	ENSP00000505206.1:n.*179+29A>T
ENST00000680791.1:n.2559A>T
ENST00000680885.1:n.5377A>T
ENST00000681158.1:c.3259A>T
ENST00000681203.1:c.3603A>T	ENSP00000506456.1:p.Gly1201=
ENST00000681371.1:n.3547A>T
ENST00000681425.1:n.4153A>T
ENST00000681639.1:n.1954A>T
ENST00000328194.7:c.3675A>T	ENSP00000328524.3:p.Gly1225=
ENST00000525784.5:c.611A>T
ENST00000527700.5:n.3237A>T
ENST00000528725.5:c.371A>T
ENST00000529977.5:n.1576A>T
ENST00000530044.5:c.3646+29A>T	ENSP00000435866.1:n.3646+29A>T
ENST00000531747.1:c.911A>T
ENST00000533737.5:c.338A>T
NM_001243254.1:c.3646+29A>T	NP_001230183.1:n.3646+29A>T
NM_015213.3:c.3675A>T	NP_056028.2:p.Gly1225=
XM_005252832.1:c.3675A>T	XP_005252889.1:p.Gly1225=
XM_011519952.1:c.3646+29A>T	XP_011518254.1:n.3646+29A>T
XM_011519953.1:c.1773A>T	XP_011518255.1:p.Gly591=
XR_242782.2:n.3857A>T
XR_930851.1:n.3828+29A>T
NM_001348749.1:c.3603A>T	NP_001335678.1:p.Gly1201=
NM_001348750.1:c.3387A>T	NP_001335679.1:p.Gly1129=
NR_145966.2:n.3849A>T
NM_015213.4:c.3675A>T MANE Select	NP_056028.2:p.Gly1225=
NM_001243254.2:c.3646+29A>T	NP_001230183.1:n.3646+29A>T
NM_001348749.2:c.3603A>T	NP_001335678.1:p.Gly1201=
NM_001348750.2:c.3387A>T	NP_001335679.1:p.Gly1129=