Canonical Allele Identifier: CA1951454079

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142026G= , CM000673.2:g.9142026G=	GRCh38
NC_000011.9:g.9163573G= , CM000673.1:g.9163573G=	GRCh37
NC_000011.8:g.9120149G=	NCBI36
NG_053019.1:g.128310C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3594C= MANE Select	ENSP00000328524.3:p.Phe1198=
ENST00000525784.6:n.1456C=
ENST00000530780.2:c.*3420C=	ENSP00000433925.1:n.*3420C=
ENST00000531747.2:n.3265C=
ENST00000679446.1:n.3515C=
ENST00000679458.1:n.4995C=
ENST00000679460.1:n.4656C=
ENST00000679568.1:c.3594C=	ENSP00000505860.1:p.Phe1198=
ENST00000679745.1:n.4099C=
ENST00000679773.1:n.2755C=
ENST00000679926.1:n.4896C=
ENST00000679999.1:c.*651C=	ENSP00000505198.1:n.*651C=
ENST00000680252.1:c.3261C=
ENST00000680294.1:c.3387C=	ENSP00000506113.1:p.Phe1129=
ENST00000680358.1:n.2893C=
ENST00000680470.1:c.*1375C=	ENSP00000505975.1:n.*1375C=
ENST00000680554.1:c.*127C=	ENSP00000505621.1:n.*127C=
ENST00000680576.1:n.5070C=
ENST00000680599.1:n.3635C=
ENST00000680742.1:c.*127C=	ENSP00000505206.1:n.*127C=
ENST00000680791.1:n.2478C=
ENST00000680885.1:n.5296C=
ENST00000681158.1:c.3178C=
ENST00000681203.1:c.3522C=	ENSP00000506456.1:p.Phe1174=
ENST00000681371.1:n.3466C=
ENST00000681425.1:n.4072C=
ENST00000681639.1:n.1873C=
ENST00000328194.7:c.3594C=	ENSP00000328524.3:p.Phe1198=
ENST00000525784.5:c.530C=
ENST00000527700.5:n.3156C=
ENST00000528725.5:c.290C=
ENST00000529977.5:n.1495C=
ENST00000530044.5:c.3594C=	ENSP00000435866.1:p.Phe1198=
ENST00000531747.1:c.830C=
ENST00000533737.5:c.257C=
NM_001243254.1:c.3594C=	NP_001230183.1:p.Phe1198=
NM_015213.3:c.3594C=	NP_056028.2:p.Phe1198=
XM_005252832.1:c.3594C=	XP_005252889.1:p.Phe1198=
XM_011519952.1:c.3594C=	XP_011518254.1:p.Phe1198=
XM_011519953.1:c.1692C=	XP_011518255.1:p.Phe564=
XR_242782.2:n.3776C=
XR_930851.1:n.3776C=
NM_001348749.1:c.3522C=	NP_001335678.1:p.Phe1174=
NM_001348750.1:c.3306C=	NP_001335679.1:p.Phe1102=
NR_145966.2:n.3768C=
NM_015213.4:c.3594C= MANE Select	NP_056028.2:p.Phe1198=
NM_001243254.2:c.3594C=	NP_001230183.1:p.Phe1198=
NM_001348749.2:c.3522C=	NP_001335678.1:p.Phe1174=
NM_001348750.2:c.3306C=	NP_001335679.1:p.Phe1102=