Canonical Allele Identifier: CA379607759
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160736T>A , CM000673.2:g.9160736T>A GRCh38
NC_000011.9:g.9182283T>A , CM000673.1:g.9182283T>A GRCh37
NC_000011.8:g.9138859T>A NCBI36
NG_053019.1:g.109600A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2413A>T MANE Select ENSP00000328524.3:p.Ser805Cys
ENST00000530780.2:c.*2239A>T ENSP00000433925.1:n.*2239A>T
ENST00000679446.1:n.2334A>T
ENST00000679458.1:n.3814A>T
ENST00000679460.1:n.2202A>T
ENST00000679568.1:c.2413A>T ENSP00000505860.1:p.Ser805Cys
ENST00000679745.1:n.2202A>T
ENST00000679926.1:n.1229A>T
ENST00000679999.1:c.2413A>T ENSP00000505198.1:p.Ser805Cys
ENST00000680252.1:c.2202A>T
ENST00000680294.1:c.2413A>T ENSP00000506113.1:p.Ser805Cys
ENST00000680358.1:n.1712A>T
ENST00000680470.1:c.*279A>T ENSP00000505975.1:n.*279A>T
ENST00000680554.1:c.2125A>T ENSP00000505621.1:p.Ser709Cys
ENST00000680576.1:n.2202A>T
ENST00000680599.1:n.2330A>T
ENST00000680742.1:c.2413A>T ENSP00000505206.1:p.Ser805Cys
ENST00000680885.1:n.2334A>T
ENST00000681158.1:c.2202A>T
ENST00000681173.1:n.2202A>T
ENST00000681203.1:c.2341A>T ENSP00000506456.1:p.Ser781Cys
ENST00000681425.1:n.2334A>T
ENST00000328194.7:c.2413A>T ENSP00000328524.3:p.Ser805Cys
ENST00000526707.5:c.2341A>T ENSP00000436780.1:p.Ser781Cys
ENST00000527700.5:n.1975A>T
ENST00000530044.5:c.2413A>T ENSP00000435866.1:p.Ser805Cys
NM_001243254.1:c.2413A>T NP_001230183.1:p.Ser805Cys
NM_015213.3:c.2413A>T NP_056028.2:p.Ser805Cys
XM_005252832.1:c.2413A>T XP_005252889.1:p.Ser805Cys
XM_011519952.1:c.2413A>T XP_011518254.1:p.Ser805Cys
XM_011519953.1:c.511A>T XP_011518255.1:p.Ser171Cys
XR_242782.2:n.2678A>T
XR_930851.1:n.2678A>T
XR_930852.1:n.2678A>T
XR_930853.1:n.2527A>T
NM_001348749.1:c.2341A>T NP_001335678.1:p.Ser781Cys
NM_001348750.1:c.2125A>T NP_001335679.1:p.Ser709Cys
NR_145966.2:n.2670A>T
NM_015213.4:c.2413A>T MANE Select NP_056028.2:p.Ser805Cys
NM_001243254.2:c.2413A>T NP_001230183.1:p.Ser805Cys
NM_001348749.2:c.2341A>T NP_001335678.1:p.Ser781Cys
NM_001348750.2:c.2125A>T NP_001335679.1:p.Ser709Cys