Canonical Allele Identifier: CA1951454045
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9141943G= , CM000673.2:g.9141943G= GRCh38
NC_000011.9:g.9163490G= , CM000673.1:g.9163490G= GRCh37
NC_000011.8:g.9120066G= NCBI36
NG_053019.1:g.128393C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.3677C= MANE Select ENSP00000328524.3:p.Ala1226=
ENST00000525784.6:n.1539C=
ENST00000530780.2:c.*3503C= ENSP00000433925.1:n.*3503C=
ENST00000531747.2:n.3348C=
ENST00000679446.1:n.3598C=
ENST00000679458.1:n.5078C=
ENST00000679460.1:n.4739C=
ENST00000679568.1:c.3677C= ENSP00000505860.1:p.Ala1226=
ENST00000679745.1:n.4182C=
ENST00000679773.1:n.2838C=
ENST00000679926.1:n.4979C=
ENST00000679999.1:c.*734C= ENSP00000505198.1:n.*734C=
ENST00000680252.1:c.3344C=
ENST00000680294.1:c.3470C= ENSP00000506113.1:p.Ala1157=
ENST00000680358.1:n.2976C=
ENST00000680470.1:c.*1458C= ENSP00000505975.1:n.*1458C=
ENST00000680554.1:c.*210C= ENSP00000505621.1:n.*210C=
ENST00000680576.1:n.5153C=
ENST00000680599.1:n.3718C=
ENST00000680742.1:c.*179+31C= ENSP00000505206.1:n.*179+31C=
ENST00000680791.1:n.2561C=
ENST00000680885.1:n.5379C=
ENST00000681158.1:c.3261C=
ENST00000681203.1:c.3605C= ENSP00000506456.1:p.Ala1202=
ENST00000681371.1:n.3549C=
ENST00000681425.1:n.4155C=
ENST00000681639.1:n.1956C=
ENST00000328194.7:c.3677C= ENSP00000328524.3:p.Ala1226=
ENST00000525784.5:c.613C=
ENST00000527700.5:n.3239C=
ENST00000528725.5:c.373C=
ENST00000529977.5:n.1578C=
ENST00000530044.5:c.3646+31C= ENSP00000435866.1:n.3646+31C=
ENST00000531747.1:c.913C=
ENST00000533737.5:c.340C=
NM_001243254.1:c.3646+31C= NP_001230183.1:n.3646+31C=
NM_015213.3:c.3677C= NP_056028.2:p.Ala1226=
XM_005252832.1:c.3677C= XP_005252889.1:p.Ala1226=
XM_011519952.1:c.3646+31C= XP_011518254.1:n.3646+31C=
XM_011519953.1:c.1775C= XP_011518255.1:p.Ala592=
XR_242782.2:n.3859C=
XR_930851.1:n.3828+31C=
NM_001348749.1:c.3605C= NP_001335678.1:p.Ala1202=
NM_001348750.1:c.3389C= NP_001335679.1:p.Ala1130=
NR_145966.2:n.3851C=
NM_015213.4:c.3677C= MANE Select NP_056028.2:p.Ala1226=
NM_001243254.2:c.3646+31C= NP_001230183.1:n.3646+31C=
NM_001348749.2:c.3605C= NP_001335678.1:p.Ala1202=
NM_001348750.2:c.3389C= NP_001335679.1:p.Ala1130=