Canonical Allele Identifier: CA1951453971

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141829A= , CM000673.2:g.9141829A=	GRCh38
NC_000011.9:g.9163376A= , CM000673.1:g.9163376A=	GRCh37
NC_000011.8:g.9119952A=	NCBI36
NG_053019.1:g.128507T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+111T= MANE Select	ENSP00000328524.3:n.3680+111T=
ENST00000525784.6:n.1542+111T=
ENST00000530780.2:c.*3506+111T=	ENSP00000433925.1:n.*3506+111T=
ENST00000531747.2:n.3351+111T=
ENST00000679446.1:n.3712T=
ENST00000679458.1:n.5081+111T=
ENST00000679460.1:n.4742+111T=
ENST00000679568.1:c.3680+111T=	ENSP00000505860.1:n.3680+111T=
ENST00000679745.1:n.4185+111T=
ENST00000679773.1:n.2841+111T=
ENST00000679926.1:n.4982+111T=
ENST00000679999.1:c.*737+111T=	ENSP00000505198.1:n.*737+111T=
ENST00000680252.1:c.3347+111T=
ENST00000680294.1:c.3473+111T=	ENSP00000506113.1:n.3473+111T=
ENST00000680358.1:n.2979+111T=
ENST00000680470.1:c.*1461+111T=	ENSP00000505975.1:n.*1461+111T=
ENST00000680554.1:c.*213+111T=	ENSP00000505621.1:n.*213+111T=
ENST00000680576.1:n.5267T=
ENST00000680599.1:n.3721+111T=
ENST00000680742.1:c.*179+145T=	ENSP00000505206.1:n.*179+145T=
ENST00000680791.1:n.2564+111T=
ENST00000680885.1:n.5382+111T=
ENST00000681158.1:c.3264+111T=
ENST00000681203.1:c.3608+111T=	ENSP00000506456.1:n.3608+111T=
ENST00000681371.1:n.3552+111T=
ENST00000681425.1:n.4158+111T=
ENST00000681639.1:n.1959+111T=
ENST00000328194.7:c.3680+111T=	ENSP00000328524.3:n.3680+111T=
ENST00000525784.5:c.616+111T=
ENST00000527700.5:n.3242+111T=
ENST00000528725.5:c.376+111T=
ENST00000529977.5:n.1581+111T=
ENST00000530044.5:c.3646+145T=	ENSP00000435866.1:n.3646+145T=
ENST00000533737.5:c.343+111T=
NM_001243254.1:c.3646+145T=	NP_001230183.1:n.3646+145T=
NM_015213.3:c.3680+111T=	NP_056028.2:n.3680+111T=
XM_005252832.1:c.3680+111T=	XP_005252889.1:n.3680+111T=
XM_011519952.1:c.3646+145T=	XP_011518254.1:n.3646+145T=
XM_011519953.1:c.1778+111T=	XP_011518255.1:n.1778+111T=
XR_242782.2:n.3862+111T=
XR_930851.1:n.3828+145T=
NM_001348749.1:c.3608+111T=	NP_001335678.1:n.3608+111T=
NM_001348750.1:c.3392+111T=	NP_001335679.1:n.3392+111T=
NR_145966.2:n.3854+111T=
NM_015213.4:c.3680+111T= MANE Select	NP_056028.2:n.3680+111T=
NM_001243254.2:c.3646+145T=	NP_001230183.1:n.3646+145T=
NM_001348749.2:c.3608+111T=	NP_001335678.1:n.3608+111T=
NM_001348750.2:c.3392+111T=	NP_001335679.1:n.3392+111T=