Canonical Allele Identifier: CA1951492120
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204301C= , CM000673.2:g.9204301C= GRCh38
NC_000011.9:g.9225848C= , CM000673.1:g.9225848C= GRCh37
NC_000011.8:g.9182424C= NCBI36
NG_053019.1:g.66035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.308G= MANE Select ENSP00000328524.3:p.Gly103=
ENST00000530780.2:c.*134G= ENSP00000433925.1:n.*134G=
ENST00000530867.2:n.97G=
ENST00000532696.2:n.231G=
ENST00000679446.1:n.229G=
ENST00000679460.1:n.97G=
ENST00000679568.1:c.308G= ENSP00000505860.1:p.Gly103=
ENST00000679745.1:n.97G=
ENST00000679999.1:c.308G= ENSP00000505198.1:p.Gly103=
ENST00000680252.1:c.97G=
ENST00000680294.1:c.308G= ENSP00000506113.1:p.Gly103=
ENST00000680470.1:c.308G= ENSP00000505975.1:p.Gly103=
ENST00000680554.1:c.20G= ENSP00000505621.1:p.Gly7=
ENST00000680576.1:n.97G=
ENST00000680599.1:n.225G=
ENST00000680742.1:c.308G= ENSP00000505206.1:p.Gly103=
ENST00000680885.1:n.229G=
ENST00000681158.1:c.97G=
ENST00000681173.1:n.97G=
ENST00000681203.1:c.236G= ENSP00000506456.1:p.Gly79=
ENST00000681425.1:n.229G=
ENST00000681915.1:n.97G=
ENST00000328194.7:c.308G= ENSP00000328524.3:p.Gly103=
ENST00000526707.5:c.236G= ENSP00000436780.1:p.Gly79=
ENST00000530044.5:c.308G= ENSP00000435866.1:p.Gly103=
ENST00000530780.1:c.*134G= ENSP00000433925.1:n.*134G=
ENST00000532696.1:n.63G=
NM_001243254.1:c.308G= NP_001230183.1:p.Gly103=
NM_015213.3:c.308G= NP_056028.2:p.Gly103=
XM_005252832.1:c.308G= XP_005252889.1:p.Gly103=
XM_011519952.1:c.308G= XP_011518254.1:p.Gly103=
XR_242782.2:n.573G=
XR_930851.1:n.573G=
XR_930852.1:n.573G=
XR_930853.1:n.573G=
NM_001348749.1:c.236G= NP_001335678.1:p.Gly79=
NM_001348750.1:c.20G= NP_001335679.1:p.Gly7=
NR_145966.2:n.565G=
NM_015213.4:c.308G= MANE Select NP_056028.2:p.Gly103=
NM_001243254.2:c.308G= NP_001230183.1:p.Gly103=
NM_001348749.2:c.236G= NP_001335678.1:p.Gly79=
NM_001348750.2:c.20G= NP_001335679.1:p.Gly7=