Canonical Allele Identifier: CA1951454096

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142059A= , CM000673.2:g.9142059A=	GRCh38
NC_000011.9:g.9163606A= , CM000673.1:g.9163606A=	GRCh37
NC_000011.8:g.9120182A=	NCBI36
NG_053019.1:g.128277T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3561T= MANE Select	ENSP00000328524.3:p.Pro1187=
ENST00000525784.6:n.1423T=
ENST00000530780.2:c.*3387T=	ENSP00000433925.1:n.*3387T=
ENST00000531747.2:n.3232T=
ENST00000679446.1:n.3482T=
ENST00000679458.1:n.4962T=
ENST00000679460.1:n.4623T=
ENST00000679568.1:c.3561T=	ENSP00000505860.1:p.Pro1187=
ENST00000679745.1:n.4066T=
ENST00000679773.1:n.2722T=
ENST00000679926.1:n.4863T=
ENST00000679999.1:c.*618T=	ENSP00000505198.1:n.*618T=
ENST00000680252.1:c.3228T=
ENST00000680294.1:c.3354T=	ENSP00000506113.1:p.Pro1118=
ENST00000680358.1:n.2860T=
ENST00000680470.1:c.*1342T=	ENSP00000505975.1:n.*1342T=
ENST00000680554.1:c.*94T=	ENSP00000505621.1:n.*94T=
ENST00000680576.1:n.5037T=
ENST00000680599.1:n.3602T=
ENST00000680742.1:c.*94T=	ENSP00000505206.1:n.*94T=
ENST00000680791.1:n.2445T=
ENST00000680885.1:n.5263T=
ENST00000681158.1:c.3145T=
ENST00000681203.1:c.3489T=	ENSP00000506456.1:p.Pro1163=
ENST00000681371.1:n.3433T=
ENST00000681425.1:n.4039T=
ENST00000681639.1:n.1840T=
ENST00000328194.7:c.3561T=	ENSP00000328524.3:p.Pro1187=
ENST00000525784.5:c.497T=
ENST00000527700.5:n.3123T=
ENST00000528725.5:c.257T=
ENST00000529977.5:n.1462T=
ENST00000530044.5:c.3561T=	ENSP00000435866.1:p.Pro1187=
ENST00000531747.1:c.797T=
ENST00000533737.5:c.224T=
NM_001243254.1:c.3561T=	NP_001230183.1:p.Pro1187=
NM_015213.3:c.3561T=	NP_056028.2:p.Pro1187=
XM_005252832.1:c.3561T=	XP_005252889.1:p.Pro1187=
XM_011519952.1:c.3561T=	XP_011518254.1:p.Pro1187=
XM_011519953.1:c.1659T=	XP_011518255.1:p.Pro553=
XR_242782.2:n.3743T=
XR_930851.1:n.3743T=
NM_001348749.1:c.3489T=	NP_001335678.1:p.Pro1163=
NM_001348750.1:c.3273T=	NP_001335679.1:p.Pro1091=
NR_145966.2:n.3735T=
NM_015213.4:c.3561T= MANE Select	NP_056028.2:p.Pro1187=
NM_001243254.2:c.3561T=	NP_001230183.1:p.Pro1187=
NM_001348749.2:c.3489T=	NP_001335678.1:p.Pro1163=
NM_001348750.2:c.3273T=	NP_001335679.1:p.Pro1091=