Canonical Allele Identifier: CA1951464362

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160731A= , CM000673.2:g.9160731A=	GRCh38
NC_000011.9:g.9182278A= , CM000673.1:g.9182278A=	GRCh37
NC_000011.8:g.9138854A=	NCBI36
NG_053019.1:g.109605T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2418T= MANE Select	ENSP00000328524.3:p.His806=
ENST00000530780.2:c.*2244T=	ENSP00000433925.1:n.*2244T=
ENST00000679446.1:n.2339T=
ENST00000679458.1:n.3819T=
ENST00000679460.1:n.2207T=
ENST00000679568.1:c.2418T=	ENSP00000505860.1:p.His806=
ENST00000679745.1:n.2207T=
ENST00000679926.1:n.1234T=
ENST00000679999.1:c.2418T=	ENSP00000505198.1:p.His806=
ENST00000680252.1:c.2207T=
ENST00000680294.1:c.2418T=	ENSP00000506113.1:p.His806=
ENST00000680358.1:n.1717T=
ENST00000680470.1:c.*284T=	ENSP00000505975.1:n.*284T=
ENST00000680554.1:c.2130T=	ENSP00000505621.1:p.His710=
ENST00000680576.1:n.2207T=
ENST00000680599.1:n.2335T=
ENST00000680742.1:c.2418T=	ENSP00000505206.1:p.His806=
ENST00000680885.1:n.2339T=
ENST00000681158.1:c.2207T=
ENST00000681173.1:n.2207T=
ENST00000681203.1:c.2346T=	ENSP00000506456.1:p.His782=
ENST00000681425.1:n.2339T=
ENST00000328194.7:c.2418T=	ENSP00000328524.3:p.His806=
ENST00000526707.5:c.2346T=	ENSP00000436780.1:p.His782=
ENST00000527700.5:n.1980T=
ENST00000530044.5:c.2418T=	ENSP00000435866.1:p.His806=
NM_001243254.1:c.2418T=	NP_001230183.1:p.His806=
NM_015213.3:c.2418T=	NP_056028.2:p.His806=
XM_005252832.1:c.2418T=	XP_005252889.1:p.His806=
XM_011519952.1:c.2418T=	XP_011518254.1:p.His806=
XM_011519953.1:c.516T=	XP_011518255.1:p.His172=
XR_242782.2:n.2683T=
XR_930851.1:n.2683T=
XR_930852.1:n.2683T=
XR_930853.1:n.2532T=
NM_001348749.1:c.2346T=	NP_001335678.1:p.His782=
NM_001348750.1:c.2130T=	NP_001335679.1:p.His710=
NR_145966.2:n.2675T=
NM_015213.4:c.2418T= MANE Select	NP_056028.2:p.His806=
NM_001243254.2:c.2418T=	NP_001230183.1:p.His806=
NM_001348749.2:c.2346T=	NP_001335678.1:p.His782=
NM_001348750.2:c.2130T=	NP_001335679.1:p.His710=