Canonical Allele Identifier: CA1951464390
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160752G= , CM000673.2:g.9160752G= GRCh38
NC_000011.9:g.9182299G= , CM000673.1:g.9182299G= GRCh37
NC_000011.8:g.9138875G= NCBI36
NG_053019.1:g.109584C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2397C= MANE Select ENSP00000328524.3:p.Leu799=
ENST00000530780.2:c.*2223C= ENSP00000433925.1:n.*2223C=
ENST00000679446.1:n.2318C=
ENST00000679458.1:n.3798C=
ENST00000679460.1:n.2186C=
ENST00000679568.1:c.2397C= ENSP00000505860.1:p.Leu799=
ENST00000679745.1:n.2186C=
ENST00000679926.1:n.1213C=
ENST00000679999.1:c.2397C= ENSP00000505198.1:p.Leu799=
ENST00000680252.1:c.2186C=
ENST00000680294.1:c.2397C= ENSP00000506113.1:p.Leu799=
ENST00000680358.1:n.1696C=
ENST00000680470.1:c.*263C= ENSP00000505975.1:n.*263C=
ENST00000680554.1:c.2109C= ENSP00000505621.1:p.Leu703=
ENST00000680576.1:n.2186C=
ENST00000680599.1:n.2314C=
ENST00000680742.1:c.2397C= ENSP00000505206.1:p.Leu799=
ENST00000680885.1:n.2318C=
ENST00000681158.1:c.2186C=
ENST00000681173.1:n.2186C=
ENST00000681203.1:c.2325C= ENSP00000506456.1:p.Leu775=
ENST00000681425.1:n.2318C=
ENST00000328194.7:c.2397C= ENSP00000328524.3:p.Leu799=
ENST00000526707.5:c.2325C= ENSP00000436780.1:p.Leu775=
ENST00000527700.5:n.1959C=
ENST00000530044.5:c.2397C= ENSP00000435866.1:p.Leu799=
NM_001243254.1:c.2397C= NP_001230183.1:p.Leu799=
NM_015213.3:c.2397C= NP_056028.2:p.Leu799=
XM_005252832.1:c.2397C= XP_005252889.1:p.Leu799=
XM_011519952.1:c.2397C= XP_011518254.1:p.Leu799=
XM_011519953.1:c.495C= XP_011518255.1:p.Leu165=
XR_242782.2:n.2662C=
XR_930851.1:n.2662C=
XR_930852.1:n.2662C=
XR_930853.1:n.2511C=
NM_001348749.1:c.2325C= NP_001335678.1:p.Leu775=
NM_001348750.1:c.2109C= NP_001335679.1:p.Leu703=
NR_145966.2:n.2654C=
NM_015213.4:c.2397C= MANE Select NP_056028.2:p.Leu799=
NM_001243254.2:c.2397C= NP_001230183.1:p.Leu799=
NM_001348749.2:c.2325C= NP_001335678.1:p.Leu775=
NM_001348750.2:c.2109C= NP_001335679.1:p.Leu703=