Canonical Allele Identifier: CA1951454064

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141986T= , CM000673.2:g.9141986T=	GRCh38
NC_000011.9:g.9163533T= , CM000673.1:g.9163533T=	GRCh37
NC_000011.8:g.9120109T=	NCBI36
NG_053019.1:g.128350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3634A= MANE Select	ENSP00000328524.3:p.Ile1212=
ENST00000525784.6:n.1496A=
ENST00000530780.2:c.*3460A=	ENSP00000433925.1:n.*3460A=
ENST00000531747.2:n.3305A=
ENST00000679446.1:n.3555A=
ENST00000679458.1:n.5035A=
ENST00000679460.1:n.4696A=
ENST00000679568.1:c.3634A=	ENSP00000505860.1:p.Ile1212=
ENST00000679745.1:n.4139A=
ENST00000679773.1:n.2795A=
ENST00000679926.1:n.4936A=
ENST00000679999.1:c.*691A=	ENSP00000505198.1:n.*691A=
ENST00000680252.1:c.3301A=
ENST00000680294.1:c.3427A=	ENSP00000506113.1:p.Ile1143=
ENST00000680358.1:n.2933A=
ENST00000680470.1:c.*1415A=	ENSP00000505975.1:n.*1415A=
ENST00000680554.1:c.*167A=	ENSP00000505621.1:n.*167A=
ENST00000680576.1:n.5110A=
ENST00000680599.1:n.3675A=
ENST00000680742.1:c.*167A=	ENSP00000505206.1:n.*167A=
ENST00000680791.1:n.2518A=
ENST00000680885.1:n.5336A=
ENST00000681158.1:c.3218A=
ENST00000681203.1:c.3562A=	ENSP00000506456.1:p.Ile1188=
ENST00000681371.1:n.3506A=
ENST00000681425.1:n.4112A=
ENST00000681639.1:n.1913A=
ENST00000328194.7:c.3634A=	ENSP00000328524.3:p.Ile1212=
ENST00000525784.5:c.570A=
ENST00000527700.5:n.3196A=
ENST00000528725.5:c.330A=
ENST00000529977.5:n.1535A=
ENST00000530044.5:c.3634A=	ENSP00000435866.1:p.Ile1212=
ENST00000531747.1:c.870A=
ENST00000533737.5:c.297A=
NM_001243254.1:c.3634A=	NP_001230183.1:p.Ile1212=
NM_015213.3:c.3634A=	NP_056028.2:p.Ile1212=
XM_005252832.1:c.3634A=	XP_005252889.1:p.Ile1212=
XM_011519952.1:c.3634A=	XP_011518254.1:p.Ile1212=
XM_011519953.1:c.1732A=	XP_011518255.1:p.Ile578=
XR_242782.2:n.3816A=
XR_930851.1:n.3816A=
NM_001348749.1:c.3562A=	NP_001335678.1:p.Ile1188=
NM_001348750.1:c.3346A=	NP_001335679.1:p.Ile1116=
NR_145966.2:n.3808A=
NM_015213.4:c.3634A= MANE Select	NP_056028.2:p.Ile1212=
NM_001243254.2:c.3634A=	NP_001230183.1:p.Ile1212=
NM_001348749.2:c.3562A=	NP_001335678.1:p.Ile1188=
NM_001348750.2:c.3346A=	NP_001335679.1:p.Ile1116=