Canonical Allele Identifier: CA1951492049
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204131C= , CM000673.2:g.9204131C= GRCh38
NC_000011.9:g.9225678C= , CM000673.1:g.9225678C= GRCh37
NC_000011.8:g.9182254C= NCBI36
NG_053019.1:g.66205G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.478G= MANE Select ENSP00000328524.3:p.Glu160=
ENST00000530780.2:c.*304G= ENSP00000433925.1:n.*304G=
ENST00000530867.2:n.267G=
ENST00000532696.2:n.401G=
ENST00000679446.1:n.399G=
ENST00000679460.1:n.267G=
ENST00000679568.1:c.478G= ENSP00000505860.1:p.Glu160=
ENST00000679745.1:n.267G=
ENST00000679999.1:c.478G= ENSP00000505198.1:p.Glu160=
ENST00000680252.1:c.267G=
ENST00000680294.1:c.478G= ENSP00000506113.1:p.Glu160=
ENST00000680470.1:c.478G= ENSP00000505975.1:p.Glu160=
ENST00000680554.1:c.190G= ENSP00000505621.1:p.Glu64=
ENST00000680576.1:n.267G=
ENST00000680599.1:n.395G=
ENST00000680742.1:c.478G= ENSP00000505206.1:p.Glu160=
ENST00000680885.1:n.399G=
ENST00000681158.1:c.267G=
ENST00000681173.1:n.267G=
ENST00000681203.1:c.406G= ENSP00000506456.1:p.Glu136=
ENST00000681425.1:n.399G=
ENST00000681915.1:n.267G=
ENST00000328194.7:c.478G= ENSP00000328524.3:p.Glu160=
ENST00000526707.5:c.406G= ENSP00000436780.1:p.Glu136=
ENST00000530044.5:c.478G= ENSP00000435866.1:p.Glu160=
ENST00000530780.1:c.*304G= ENSP00000433925.1:n.*304G=
ENST00000532696.1:n.233G=
NM_001243254.1:c.478G= NP_001230183.1:p.Glu160=
NM_015213.3:c.478G= NP_056028.2:p.Glu160=
XM_005252832.1:c.478G= XP_005252889.1:p.Glu160=
XM_011519952.1:c.478G= XP_011518254.1:p.Glu160=
XR_242782.2:n.743G=
XR_930851.1:n.743G=
XR_930852.1:n.743G=
XR_930853.1:n.743G=
NM_001348749.1:c.406G= NP_001335678.1:p.Glu136=
NM_001348750.1:c.190G= NP_001335679.1:p.Glu64=
NR_145966.2:n.735G=
NM_015213.4:c.478G= MANE Select NP_056028.2:p.Glu160=
NM_001243254.2:c.478G= NP_001230183.1:p.Glu160=
NM_001348749.2:c.406G= NP_001335678.1:p.Glu136=
NM_001348750.2:c.190G= NP_001335679.1:p.Glu64=