Canonical Allele Identifier: CA1951464365
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160737C= , CM000673.2:g.9160737C= GRCh38
NC_000011.9:g.9182284C= , CM000673.1:g.9182284C= GRCh37
NC_000011.8:g.9138860C= NCBI36
NG_053019.1:g.109599G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2412G= MANE Select ENSP00000328524.3:p.Trp804=
ENST00000530780.2:c.*2238G= ENSP00000433925.1:n.*2238G=
ENST00000679446.1:n.2333G=
ENST00000679458.1:n.3813G=
ENST00000679460.1:n.2201G=
ENST00000679568.1:c.2412G= ENSP00000505860.1:p.Trp804=
ENST00000679745.1:n.2201G=
ENST00000679926.1:n.1228G=
ENST00000679999.1:c.2412G= ENSP00000505198.1:p.Trp804=
ENST00000680252.1:c.2201G=
ENST00000680294.1:c.2412G= ENSP00000506113.1:p.Trp804=
ENST00000680358.1:n.1711G=
ENST00000680470.1:c.*278G= ENSP00000505975.1:n.*278G=
ENST00000680554.1:c.2124G= ENSP00000505621.1:p.Trp708=
ENST00000680576.1:n.2201G=
ENST00000680599.1:n.2329G=
ENST00000680742.1:c.2412G= ENSP00000505206.1:p.Trp804=
ENST00000680885.1:n.2333G=
ENST00000681158.1:c.2201G=
ENST00000681173.1:n.2201G=
ENST00000681203.1:c.2340G= ENSP00000506456.1:p.Trp780=
ENST00000681425.1:n.2333G=
ENST00000328194.7:c.2412G= ENSP00000328524.3:p.Trp804=
ENST00000526707.5:c.2340G= ENSP00000436780.1:p.Trp780=
ENST00000527700.5:n.1974G=
ENST00000530044.5:c.2412G= ENSP00000435866.1:p.Trp804=
NM_001243254.1:c.2412G= NP_001230183.1:p.Trp804=
NM_015213.3:c.2412G= NP_056028.2:p.Trp804=
XM_005252832.1:c.2412G= XP_005252889.1:p.Trp804=
XM_011519952.1:c.2412G= XP_011518254.1:p.Trp804=
XM_011519953.1:c.510G= XP_011518255.1:p.Trp170=
XR_242782.2:n.2677G=
XR_930851.1:n.2677G=
XR_930852.1:n.2677G=
XR_930853.1:n.2526G=
NM_001348749.1:c.2340G= NP_001335678.1:p.Trp780=
NM_001348750.1:c.2124G= NP_001335679.1:p.Trp708=
NR_145966.2:n.2669G=
NM_015213.4:c.2412G= MANE Select NP_056028.2:p.Trp804=
NM_001243254.2:c.2412G= NP_001230183.1:p.Trp804=
NM_001348749.2:c.2340G= NP_001335678.1:p.Trp780=
NM_001348750.2:c.2124G= NP_001335679.1:p.Trp708=