Canonical Allele Identifier: CA1951492099
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204258G= , CM000673.2:g.9204258G= GRCh38
NC_000011.9:g.9225805G= , CM000673.1:g.9225805G= GRCh37
NC_000011.8:g.9182381G= NCBI36
NG_053019.1:g.66078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.351C= MANE Select ENSP00000328524.3:p.Phe117=
ENST00000530780.2:c.*177C= ENSP00000433925.1:n.*177C=
ENST00000530867.2:n.140C=
ENST00000532696.2:n.274C=
ENST00000679446.1:n.272C=
ENST00000679460.1:n.140C=
ENST00000679568.1:c.351C= ENSP00000505860.1:p.Phe117=
ENST00000679745.1:n.140C=
ENST00000679999.1:c.351C= ENSP00000505198.1:p.Phe117=
ENST00000680252.1:c.140C=
ENST00000680294.1:c.351C= ENSP00000506113.1:p.Phe117=
ENST00000680470.1:c.351C= ENSP00000505975.1:p.Phe117=
ENST00000680554.1:c.63C= ENSP00000505621.1:p.Phe21=
ENST00000680576.1:n.140C=
ENST00000680599.1:n.268C=
ENST00000680742.1:c.351C= ENSP00000505206.1:p.Phe117=
ENST00000680885.1:n.272C=
ENST00000681158.1:c.140C=
ENST00000681173.1:n.140C=
ENST00000681203.1:c.279C= ENSP00000506456.1:p.Phe93=
ENST00000681425.1:n.272C=
ENST00000681915.1:n.140C=
ENST00000328194.7:c.351C= ENSP00000328524.3:p.Phe117=
ENST00000526707.5:c.279C= ENSP00000436780.1:p.Phe93=
ENST00000530044.5:c.351C= ENSP00000435866.1:p.Phe117=
ENST00000530780.1:c.*177C= ENSP00000433925.1:n.*177C=
ENST00000532696.1:n.106C=
NM_001243254.1:c.351C= NP_001230183.1:p.Phe117=
NM_015213.3:c.351C= NP_056028.2:p.Phe117=
XM_005252832.1:c.351C= XP_005252889.1:p.Phe117=
XM_011519952.1:c.351C= XP_011518254.1:p.Phe117=
XR_242782.2:n.616C=
XR_930851.1:n.616C=
XR_930852.1:n.616C=
XR_930853.1:n.616C=
NM_001348749.1:c.279C= NP_001335678.1:p.Phe93=
NM_001348750.1:c.63C= NP_001335679.1:p.Phe21=
NR_145966.2:n.608C=
NM_015213.4:c.351C= MANE Select NP_056028.2:p.Phe117=
NM_001243254.2:c.351C= NP_001230183.1:p.Phe117=
NM_001348749.2:c.279C= NP_001335678.1:p.Phe93=
NM_001348750.2:c.63C= NP_001335679.1:p.Phe21=