Canonical Allele Identifier: CA1951454088

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142043T= , CM000673.2:g.9142043T=	GRCh38
NC_000011.9:g.9163590T= , CM000673.1:g.9163590T=	GRCh37
NC_000011.8:g.9120166T=	NCBI36
NG_053019.1:g.128293A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3577A= MANE Select	ENSP00000328524.3:p.Thr1193=
ENST00000525784.6:n.1439A=
ENST00000530780.2:c.*3403A=	ENSP00000433925.1:n.*3403A=
ENST00000531747.2:n.3248A=
ENST00000679446.1:n.3498A=
ENST00000679458.1:n.4978A=
ENST00000679460.1:n.4639A=
ENST00000679568.1:c.3577A=	ENSP00000505860.1:p.Thr1193=
ENST00000679745.1:n.4082A=
ENST00000679773.1:n.2738A=
ENST00000679926.1:n.4879A=
ENST00000679999.1:c.*634A=	ENSP00000505198.1:n.*634A=
ENST00000680252.1:c.3244A=
ENST00000680294.1:c.3370A=	ENSP00000506113.1:p.Thr1124=
ENST00000680358.1:n.2876A=
ENST00000680470.1:c.*1358A=	ENSP00000505975.1:n.*1358A=
ENST00000680554.1:c.*110A=	ENSP00000505621.1:n.*110A=
ENST00000680576.1:n.5053A=
ENST00000680599.1:n.3618A=
ENST00000680742.1:c.*110A=	ENSP00000505206.1:n.*110A=
ENST00000680791.1:n.2461A=
ENST00000680885.1:n.5279A=
ENST00000681158.1:c.3161A=
ENST00000681203.1:c.3505A=	ENSP00000506456.1:p.Thr1169=
ENST00000681371.1:n.3449A=
ENST00000681425.1:n.4055A=
ENST00000681639.1:n.1856A=
ENST00000328194.7:c.3577A=	ENSP00000328524.3:p.Thr1193=
ENST00000525784.5:c.513A=
ENST00000527700.5:n.3139A=
ENST00000528725.5:c.273A=
ENST00000529977.5:n.1478A=
ENST00000530044.5:c.3577A=	ENSP00000435866.1:p.Thr1193=
ENST00000531747.1:c.813A=
ENST00000533737.5:c.240A=
NM_001243254.1:c.3577A=	NP_001230183.1:p.Thr1193=
NM_015213.3:c.3577A=	NP_056028.2:p.Thr1193=
XM_005252832.1:c.3577A=	XP_005252889.1:p.Thr1193=
XM_011519952.1:c.3577A=	XP_011518254.1:p.Thr1193=
XM_011519953.1:c.1675A=	XP_011518255.1:p.Thr559=
XR_242782.2:n.3759A=
XR_930851.1:n.3759A=
NM_001348749.1:c.3505A=	NP_001335678.1:p.Thr1169=
NM_001348750.1:c.3289A=	NP_001335679.1:p.Thr1097=
NR_145966.2:n.3751A=
NM_015213.4:c.3577A= MANE Select	NP_056028.2:p.Thr1193=
NM_001243254.2:c.3577A=	NP_001230183.1:p.Thr1193=
NM_001348749.2:c.3505A=	NP_001335678.1:p.Thr1169=
NM_001348750.2:c.3289A=	NP_001335679.1:p.Thr1097=