Canonical Allele Identifier: CA1747608878

Gene: DENND2A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140531330C= , CM000669.2:g.140531330C=	GRCh38
NC_000007.13:g.140231130C= , CM000669.1:g.140231130C=	GRCh37
NC_000007.12:g.139877599C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015689.5:c.2328-3835G= MANE Select	NP_056504.3:n.2328-3835G=
ENST00000496613.6:c.2328-3835G= MANE Select	ENSP00000419654.1:n.2328-3835G=
NM_001318052.1:c.2328-3835G=	NP_001304981.1:n.2328-3835G=
NM_001318052.2:c.2328-3835G=	NP_001304981.1:n.2328-3835G=
NM_001362678.1:c.2328-3835G=	NP_001349607.1:n.2328-3835G=
NM_001362678.2:c.2328-3835G=	NP_001349607.1:n.2328-3835G=
NM_015689.3:c.2328-3835G=	NP_056504.3:n.2328-3835G=
NM_015689.4:c.2328-3835G=	NP_056504.3:n.2328-3835G=
NR_134477.1:n.2473-3893G=
ENST00000275884.10:c.2328-3835G=	ENSP00000275884.6:n.2328-3835G=
ENST00000461883.5:c.2328-3893G=	ENSP00000417673.1:n.2328-3893G=
ENST00000469373.5:c.369-3893G=	ENSP00000420145.1:n.369-3893G=
ENST00000496613.5:c.2328-3835G=	ENSP00000419654.1:n.2328-3835G=
ENST00000537639.5:c.2328-3835G=	ENSP00000442245.1:n.2328-3835G=
XM_005249976.3:c.2328-3835G=	XP_005250033.1:n.2328-3835G=
XM_005249977.2:c.2328-3835G=	XP_005250034.1:n.2328-3835G=
XM_005249978.3:c.2328-3835G=	XP_005250035.1:n.2328-3835G=
XM_011516052.1:c.2328-3835G=	XP_011514354.1:n.2328-3835G=
XM_011516053.1:c.2328-3835G=	XP_011514355.1:n.2328-3835G=
XM_011516053.2:c.2328-3835G=	XP_011514355.1:n.2328-3835G=
XM_011516054.1:c.2325-3835G=	XP_011514356.1:n.2325-3835G=
XM_011516054.2:c.2325-3835G=	XP_011514356.1:n.2325-3835G=
XM_017011989.1:c.2328-3835G=	XP_016867478.1:n.2328-3835G=