Canonical Allele Identifier: CA1951454110

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142083T= , CM000673.2:g.9142083T=	GRCh38
NC_000011.9:g.9163630T= , CM000673.1:g.9163630T=	GRCh37
NC_000011.8:g.9120206T=	NCBI36
NG_053019.1:g.128253A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3537A= MANE Select	ENSP00000328524.3:p.Thr1179=
ENST00000525784.6:n.1399A=
ENST00000530780.2:c.*3363A=	ENSP00000433925.1:n.*3363A=
ENST00000531747.2:n.3208A=
ENST00000679446.1:n.3458A=
ENST00000679458.1:n.4938A=
ENST00000679460.1:n.4599A=
ENST00000679568.1:c.3537A=	ENSP00000505860.1:p.Thr1179=
ENST00000679745.1:n.4042A=
ENST00000679773.1:n.2698A=
ENST00000679926.1:n.4839A=
ENST00000679999.1:c.*594A=	ENSP00000505198.1:n.*594A=
ENST00000680252.1:c.3204A=
ENST00000680294.1:c.3330A=	ENSP00000506113.1:p.Thr1110=
ENST00000680358.1:n.2836A=
ENST00000680470.1:c.*1318A=	ENSP00000505975.1:n.*1318A=
ENST00000680554.1:c.*70A=	ENSP00000505621.1:n.*70A=
ENST00000680576.1:n.5013A=
ENST00000680599.1:n.3578A=
ENST00000680742.1:c.*70A=	ENSP00000505206.1:n.*70A=
ENST00000680791.1:n.2421A=
ENST00000680885.1:n.5239A=
ENST00000681158.1:c.3121A=
ENST00000681203.1:c.3465A=	ENSP00000506456.1:p.Thr1155=
ENST00000681371.1:n.3409A=
ENST00000681425.1:n.4015A=
ENST00000681639.1:n.1816A=
ENST00000328194.7:c.3537A=	ENSP00000328524.3:p.Thr1179=
ENST00000525784.5:c.473A=
ENST00000527700.5:n.3099A=
ENST00000528725.5:c.233A=
ENST00000529977.5:n.1438A=
ENST00000530044.5:c.3537A=	ENSP00000435866.1:p.Thr1179=
ENST00000531747.1:c.773A=
ENST00000533737.5:c.200A=
NM_001243254.1:c.3537A=	NP_001230183.1:p.Thr1179=
NM_015213.3:c.3537A=	NP_056028.2:p.Thr1179=
XM_005252832.1:c.3537A=	XP_005252889.1:p.Thr1179=
XM_011519952.1:c.3537A=	XP_011518254.1:p.Thr1179=
XM_011519953.1:c.1635A=	XP_011518255.1:p.Thr545=
XR_242782.2:n.3719A=
XR_930851.1:n.3719A=
NM_001348749.1:c.3465A=	NP_001335678.1:p.Thr1155=
NM_001348750.1:c.3249A=	NP_001335679.1:p.Thr1083=
NR_145966.2:n.3711A=
NM_015213.4:c.3537A= MANE Select	NP_056028.2:p.Thr1179=
NM_001243254.2:c.3537A=	NP_001230183.1:p.Thr1179=
NM_001348749.2:c.3465A=	NP_001335678.1:p.Thr1155=
NM_001348750.2:c.3249A=	NP_001335679.1:p.Thr1083=