Canonical Allele Identifier: CA1951454116

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142097T= , CM000673.2:g.9142097T=	GRCh38
NC_000011.9:g.9163644T= , CM000673.1:g.9163644T=	GRCh37
NC_000011.8:g.9120220T=	NCBI36
NG_053019.1:g.128239A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3523A= MANE Select	ENSP00000328524.3:p.Thr1175=
ENST00000525784.6:n.1385A=
ENST00000530780.2:c.*3349A=	ENSP00000433925.1:n.*3349A=
ENST00000531747.2:n.3194A=
ENST00000679446.1:n.3444A=
ENST00000679458.1:n.4924A=
ENST00000679460.1:n.4585A=
ENST00000679568.1:c.3523A=	ENSP00000505860.1:p.Thr1175=
ENST00000679745.1:n.4028A=
ENST00000679773.1:n.2684A=
ENST00000679926.1:n.4825A=
ENST00000679999.1:c.*580A=	ENSP00000505198.1:n.*580A=
ENST00000680252.1:c.3190A=
ENST00000680294.1:c.3316A=	ENSP00000506113.1:p.Thr1106=
ENST00000680358.1:n.2822A=
ENST00000680470.1:c.*1304A=	ENSP00000505975.1:n.*1304A=
ENST00000680554.1:c.*56A=	ENSP00000505621.1:n.*56A=
ENST00000680576.1:n.4999A=
ENST00000680599.1:n.3564A=
ENST00000680742.1:c.*56A=	ENSP00000505206.1:n.*56A=
ENST00000680791.1:n.2407A=
ENST00000680885.1:n.5225A=
ENST00000681158.1:c.3107A=
ENST00000681203.1:c.3451A=	ENSP00000506456.1:p.Thr1151=
ENST00000681371.1:n.3395A=
ENST00000681425.1:n.4001A=
ENST00000681639.1:n.1802A=
ENST00000328194.7:c.3523A=	ENSP00000328524.3:p.Thr1175=
ENST00000525784.5:c.459A=
ENST00000527700.5:n.3085A=
ENST00000528725.5:c.219A=
ENST00000529977.5:n.1424A=
ENST00000530044.5:c.3523A=	ENSP00000435866.1:p.Thr1175=
ENST00000531747.1:c.759A=
ENST00000533737.5:c.186A=
NM_001243254.1:c.3523A=	NP_001230183.1:p.Thr1175=
NM_015213.3:c.3523A=	NP_056028.2:p.Thr1175=
XM_005252832.1:c.3523A=	XP_005252889.1:p.Thr1175=
XM_011519952.1:c.3523A=	XP_011518254.1:p.Thr1175=
XM_011519953.1:c.1621A=	XP_011518255.1:p.Thr541=
XR_242782.2:n.3705A=
XR_930851.1:n.3705A=
NM_001348749.1:c.3451A=	NP_001335678.1:p.Thr1151=
NM_001348750.1:c.3235A=	NP_001335679.1:p.Thr1079=
NR_145966.2:n.3697A=
NM_015213.4:c.3523A= MANE Select	NP_056028.2:p.Thr1175=
NM_001243254.2:c.3523A=	NP_001230183.1:p.Thr1175=
NM_001348749.2:c.3451A=	NP_001335678.1:p.Thr1151=
NM_001348750.2:c.3235A=	NP_001335679.1:p.Thr1079=