Canonical Allele Identifier: CA379608164
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160786T>A , CM000673.2:g.9160786T>A GRCh38
NC_000011.9:g.9182333T>A , CM000673.1:g.9182333T>A GRCh37
NC_000011.8:g.9138909T>A NCBI36
NG_053019.1:g.109550A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2363A>T MANE Select ENSP00000328524.3:p.Glu788Val
ENST00000530780.2:c.*2189A>T ENSP00000433925.1:n.*2189A>T
ENST00000679446.1:n.2284A>T
ENST00000679458.1:n.3764A>T
ENST00000679460.1:n.2152A>T
ENST00000679568.1:c.2363A>T ENSP00000505860.1:p.Glu788Val
ENST00000679745.1:n.2152A>T
ENST00000679926.1:n.1179A>T
ENST00000679999.1:c.2363A>T ENSP00000505198.1:p.Glu788Val
ENST00000680252.1:c.2152A>T
ENST00000680294.1:c.2363A>T ENSP00000506113.1:p.Glu788Val
ENST00000680358.1:n.1662A>T
ENST00000680470.1:c.*229A>T ENSP00000505975.1:n.*229A>T
ENST00000680554.1:c.2075A>T ENSP00000505621.1:p.Glu692Val
ENST00000680576.1:n.2152A>T
ENST00000680599.1:n.2280A>T
ENST00000680742.1:c.2363A>T ENSP00000505206.1:p.Glu788Val
ENST00000680885.1:n.2284A>T
ENST00000681158.1:c.2152A>T
ENST00000681173.1:n.2152A>T
ENST00000681203.1:c.2291A>T ENSP00000506456.1:p.Glu764Val
ENST00000681425.1:n.2284A>T
ENST00000328194.7:c.2363A>T ENSP00000328524.3:p.Glu788Val
ENST00000526707.5:c.2291A>T ENSP00000436780.1:p.Glu764Val
ENST00000527700.5:n.1925A>T
ENST00000530044.5:c.2363A>T ENSP00000435866.1:p.Glu788Val
NM_001243254.1:c.2363A>T NP_001230183.1:p.Glu788Val
NM_015213.3:c.2363A>T NP_056028.2:p.Glu788Val
XM_005252832.1:c.2363A>T XP_005252889.1:p.Glu788Val
XM_011519952.1:c.2363A>T XP_011518254.1:p.Glu788Val
XM_011519953.1:c.461A>T XP_011518255.1:p.Glu154Val
XR_242782.2:n.2628A>T
XR_930851.1:n.2628A>T
XR_930852.1:n.2628A>T
XR_930853.1:n.2477A>T
NM_001348749.1:c.2291A>T NP_001335678.1:p.Glu764Val
NM_001348750.1:c.2075A>T NP_001335679.1:p.Glu692Val
NR_145966.2:n.2620A>T
NM_015213.4:c.2363A>T MANE Select NP_056028.2:p.Glu788Val
NM_001243254.2:c.2363A>T NP_001230183.1:p.Glu788Val
NM_001348749.2:c.2291A>T NP_001335678.1:p.Glu764Val
NM_001348750.2:c.2075A>T NP_001335679.1:p.Glu692Val