Canonical Allele Identifier: CA1951454087

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142042G= , CM000673.2:g.9142042G=	GRCh38
NC_000011.9:g.9163589G= , CM000673.1:g.9163589G=	GRCh37
NC_000011.8:g.9120165G=	NCBI36
NG_053019.1:g.128294C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3578C= MANE Select	ENSP00000328524.3:p.Thr1193=
ENST00000525784.6:n.1440C=
ENST00000530780.2:c.*3404C=	ENSP00000433925.1:n.*3404C=
ENST00000531747.2:n.3249C=
ENST00000679446.1:n.3499C=
ENST00000679458.1:n.4979C=
ENST00000679460.1:n.4640C=
ENST00000679568.1:c.3578C=	ENSP00000505860.1:p.Thr1193=
ENST00000679745.1:n.4083C=
ENST00000679773.1:n.2739C=
ENST00000679926.1:n.4880C=
ENST00000679999.1:c.*635C=	ENSP00000505198.1:n.*635C=
ENST00000680252.1:c.3245C=
ENST00000680294.1:c.3371C=	ENSP00000506113.1:p.Thr1124=
ENST00000680358.1:n.2877C=
ENST00000680470.1:c.*1359C=	ENSP00000505975.1:n.*1359C=
ENST00000680554.1:c.*111C=	ENSP00000505621.1:n.*111C=
ENST00000680576.1:n.5054C=
ENST00000680599.1:n.3619C=
ENST00000680742.1:c.*111C=	ENSP00000505206.1:n.*111C=
ENST00000680791.1:n.2462C=
ENST00000680885.1:n.5280C=
ENST00000681158.1:c.3162C=
ENST00000681203.1:c.3506C=	ENSP00000506456.1:p.Thr1169=
ENST00000681371.1:n.3450C=
ENST00000681425.1:n.4056C=
ENST00000681639.1:n.1857C=
ENST00000328194.7:c.3578C=	ENSP00000328524.3:p.Thr1193=
ENST00000525784.5:c.514C=
ENST00000527700.5:n.3140C=
ENST00000528725.5:c.274C=
ENST00000529977.5:n.1479C=
ENST00000530044.5:c.3578C=	ENSP00000435866.1:p.Thr1193=
ENST00000531747.1:c.814C=
ENST00000533737.5:c.241C=
NM_001243254.1:c.3578C=	NP_001230183.1:p.Thr1193=
NM_015213.3:c.3578C=	NP_056028.2:p.Thr1193=
XM_005252832.1:c.3578C=	XP_005252889.1:p.Thr1193=
XM_011519952.1:c.3578C=	XP_011518254.1:p.Thr1193=
XM_011519953.1:c.1676C=	XP_011518255.1:p.Thr559=
XR_242782.2:n.3760C=
XR_930851.1:n.3760C=
NM_001348749.1:c.3506C=	NP_001335678.1:p.Thr1169=
NM_001348750.1:c.3290C=	NP_001335679.1:p.Thr1097=
NR_145966.2:n.3752C=
NM_015213.4:c.3578C= MANE Select	NP_056028.2:p.Thr1193=
NM_001243254.2:c.3578C=	NP_001230183.1:p.Thr1193=
NM_001348749.2:c.3506C=	NP_001335678.1:p.Thr1169=
NM_001348750.2:c.3290C=	NP_001335679.1:p.Thr1097=