Canonical Allele Identifier: CA1951464400
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160758A= , CM000673.2:g.9160758A= GRCh38
NC_000011.9:g.9182305A= , CM000673.1:g.9182305A= GRCh37
NC_000011.8:g.9138881A= NCBI36
NG_053019.1:g.109578T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2391T= MANE Select ENSP00000328524.3:p.Cys797=
ENST00000530780.2:c.*2217T= ENSP00000433925.1:n.*2217T=
ENST00000679446.1:n.2312T=
ENST00000679458.1:n.3792T=
ENST00000679460.1:n.2180T=
ENST00000679568.1:c.2391T= ENSP00000505860.1:p.Cys797=
ENST00000679745.1:n.2180T=
ENST00000679926.1:n.1207T=
ENST00000679999.1:c.2391T= ENSP00000505198.1:p.Cys797=
ENST00000680252.1:c.2180T=
ENST00000680294.1:c.2391T= ENSP00000506113.1:p.Cys797=
ENST00000680358.1:n.1690T=
ENST00000680470.1:c.*257T= ENSP00000505975.1:n.*257T=
ENST00000680554.1:c.2103T= ENSP00000505621.1:p.Cys701=
ENST00000680576.1:n.2180T=
ENST00000680599.1:n.2308T=
ENST00000680742.1:c.2391T= ENSP00000505206.1:p.Cys797=
ENST00000680885.1:n.2312T=
ENST00000681158.1:c.2180T=
ENST00000681173.1:n.2180T=
ENST00000681203.1:c.2319T= ENSP00000506456.1:p.Cys773=
ENST00000681425.1:n.2312T=
ENST00000328194.7:c.2391T= ENSP00000328524.3:p.Cys797=
ENST00000526707.5:c.2319T= ENSP00000436780.1:p.Cys773=
ENST00000527700.5:n.1953T=
ENST00000530044.5:c.2391T= ENSP00000435866.1:p.Cys797=
NM_001243254.1:c.2391T= NP_001230183.1:p.Cys797=
NM_015213.3:c.2391T= NP_056028.2:p.Cys797=
XM_005252832.1:c.2391T= XP_005252889.1:p.Cys797=
XM_011519952.1:c.2391T= XP_011518254.1:p.Cys797=
XM_011519953.1:c.489T= XP_011518255.1:p.Cys163=
XR_242782.2:n.2656T=
XR_930851.1:n.2656T=
XR_930852.1:n.2656T=
XR_930853.1:n.2505T=
NM_001348749.1:c.2319T= NP_001335678.1:p.Cys773=
NM_001348750.1:c.2103T= NP_001335679.1:p.Cys701=
NR_145966.2:n.2648T=
NM_015213.4:c.2391T= MANE Select NP_056028.2:p.Cys797=
NM_001243254.2:c.2391T= NP_001230183.1:p.Cys797=
NM_001348749.2:c.2319T= NP_001335678.1:p.Cys773=
NM_001348750.2:c.2103T= NP_001335679.1:p.Cys701=