Canonical Allele Identifier: CA1951452986

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9139724G= , CM000673.2:g.9139724G=	GRCh38
NC_000011.9:g.9161271G= , CM000673.1:g.9161271G=	GRCh37
NC_000011.8:g.9117847G=	NCBI36
NG_053019.1:g.130612C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3811C= MANE Select	ENSP00000328524.3:p.Gln1271=
ENST00000525784.6:n.1673C=
ENST00000530780.2:c.*3637C=	ENSP00000433925.1:n.*3637C=
ENST00000531747.2:n.3482C=
ENST00000679446.1:n.5817C=
ENST00000679458.1:n.5212C=
ENST00000679460.1:n.4873C=
ENST00000679568.1:c.3871C=	ENSP00000505860.1:p.Gln1291=
ENST00000679745.1:n.4316C=
ENST00000679773.1:n.2972C=
ENST00000679926.1:n.5113C=
ENST00000679999.1:c.*868C=	ENSP00000505198.1:n.*868C=
ENST00000680252.1:c.3478C=
ENST00000680294.1:c.3604C=	ENSP00000506113.1:p.Gln1202=
ENST00000680358.1:n.3110C=
ENST00000680470.1:c.*1592C=	ENSP00000505975.1:n.*1592C=
ENST00000680554.1:c.*344C=	ENSP00000505621.1:n.*344C=
ENST00000680576.1:n.7372C=
ENST00000680599.1:n.3852C=
ENST00000680742.1:c.*310C=	ENSP00000505206.1:n.*310C=
ENST00000680791.1:n.2695C=
ENST00000680885.1:n.5513C=
ENST00000681158.1:c.3395C=
ENST00000681203.1:c.3739C=	ENSP00000506456.1:p.Gln1247=
ENST00000681371.1:n.3683C=
ENST00000681425.1:n.4289C=
ENST00000681639.1:n.2090C=
ENST00000328194.7:c.3811C=	ENSP00000328524.3:p.Gln1271=
ENST00000525784.5:c.747C=
ENST00000527700.5:n.3373C=
ENST00000528725.5:c.507C=
ENST00000529977.5:n.1712C=
ENST00000530044.5:c.*51C=	ENSP00000435866.1:n.*51C=
ENST00000533737.5:c.534C=
NM_001243254.1:c.*51C=	NP_001230183.1:n.*51C=
NM_015213.3:c.3811C=	NP_056028.2:p.Gln1271=
XM_005252832.1:c.3871C=	XP_005252889.1:p.Gln1291=
XM_011519953.1:c.1969C=	XP_011518255.1:p.Gln657=
XR_242782.2:n.3993C=
XR_930851.1:n.3959C=
NM_001348749.1:c.3739C=	NP_001335678.1:p.Gln1247=
NM_001348750.1:c.3523C=	NP_001335679.1:p.Gln1175=
NR_145966.2:n.3985C=
NM_015213.4:c.3811C= MANE Select	NP_056028.2:p.Gln1271=
NM_001243254.2:c.*51C=	NP_001230183.1:n.*51C=
NM_001348749.2:c.3739C=	NP_001335678.1:p.Gln1247=
NM_001348750.2:c.3523C=	NP_001335679.1:p.Gln1175=