Canonical Allele Identifier: CA1951454059

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141973C= , CM000673.2:g.9141973C=	GRCh38
NC_000011.9:g.9163520C= , CM000673.1:g.9163520C=	GRCh37
NC_000011.8:g.9120096C=	NCBI36
NG_053019.1:g.128363G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3647G= MANE Select	ENSP00000328524.3:p.Gly1216=
ENST00000525784.6:n.1509G=
ENST00000530780.2:c.*3473G=	ENSP00000433925.1:n.*3473G=
ENST00000531747.2:n.3318G=
ENST00000679446.1:n.3568G=
ENST00000679458.1:n.5048G=
ENST00000679460.1:n.4709G=
ENST00000679568.1:c.3647G=	ENSP00000505860.1:p.Gly1216=
ENST00000679745.1:n.4152G=
ENST00000679773.1:n.2808G=
ENST00000679926.1:n.4949G=
ENST00000679999.1:c.*704G=	ENSP00000505198.1:n.*704G=
ENST00000680252.1:c.3314G=
ENST00000680294.1:c.3440G=	ENSP00000506113.1:p.Gly1147=
ENST00000680358.1:n.2946G=
ENST00000680470.1:c.*1428G=	ENSP00000505975.1:n.*1428G=
ENST00000680554.1:c.*180G=	ENSP00000505621.1:n.*180G=
ENST00000680576.1:n.5123G=
ENST00000680599.1:n.3688G=
ENST00000680742.1:c.*179+1G=	ENSP00000505206.1:n.*179+1G=
ENST00000680791.1:n.2531G=
ENST00000680885.1:n.5349G=
ENST00000681158.1:c.3231G=
ENST00000681203.1:c.3575G=	ENSP00000506456.1:p.Gly1192=
ENST00000681371.1:n.3519G=
ENST00000681425.1:n.4125G=
ENST00000681639.1:n.1926G=
ENST00000328194.7:c.3647G=	ENSP00000328524.3:p.Gly1216=
ENST00000525784.5:c.583G=
ENST00000527700.5:n.3209G=
ENST00000528725.5:c.343G=
ENST00000529977.5:n.1548G=
ENST00000530044.5:c.3646+1G=	ENSP00000435866.1:n.3646+1G=
ENST00000531747.1:c.883G=
ENST00000533737.5:c.310G=
NM_001243254.1:c.3646+1G=	NP_001230183.1:n.3646+1G=
NM_015213.3:c.3647G=	NP_056028.2:p.Gly1216=
XM_005252832.1:c.3647G=	XP_005252889.1:p.Gly1216=
XM_011519952.1:c.3646+1G=	XP_011518254.1:n.3646+1G=
XM_011519953.1:c.1745G=	XP_011518255.1:p.Gly582=
XR_242782.2:n.3829G=
XR_930851.1:n.3828+1G=
NM_001348749.1:c.3575G=	NP_001335678.1:p.Gly1192=
NM_001348750.1:c.3359G=	NP_001335679.1:p.Gly1120=
NR_145966.2:n.3821G=
NM_015213.4:c.3647G= MANE Select	NP_056028.2:p.Gly1216=
NM_001243254.2:c.3646+1G=	NP_001230183.1:n.3646+1G=
NM_001348749.2:c.3575G=	NP_001335678.1:p.Gly1192=
NM_001348750.2:c.3359G=	NP_001335679.1:p.Gly1120=