Canonical Allele Identifier: CA379607679
Gene: DENND5A HGNC NCBI

Linked Data

dbSNP Id: rs1590218477

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160723T>A , CM000673.2:g.9160723T>A GRCh38
NC_000011.9:g.9182270T>A , CM000673.1:g.9182270T>A GRCh37
NC_000011.8:g.9138846T>A NCBI36
NG_053019.1:g.109613A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2426A>T MANE Select ENSP00000328524.3:p.Gln809Leu
ENST00000530780.2:c.*2252A>T ENSP00000433925.1:n.*2252A>T
ENST00000679446.1:n.2347A>T
ENST00000679458.1:n.3827A>T
ENST00000679460.1:n.2215A>T
ENST00000679568.1:c.2426A>T ENSP00000505860.1:p.Gln809Leu
ENST00000679745.1:n.2215A>T
ENST00000679926.1:n.1242A>T
ENST00000679999.1:c.2426A>T ENSP00000505198.1:p.Gln809Leu
ENST00000680252.1:c.2215A>T
ENST00000680294.1:c.2426A>T ENSP00000506113.1:p.Gln809Leu
ENST00000680358.1:n.1725A>T
ENST00000680470.1:c.*292A>T ENSP00000505975.1:n.*292A>T
ENST00000680554.1:c.2138A>T ENSP00000505621.1:p.Gln713Leu
ENST00000680576.1:n.2215A>T
ENST00000680599.1:n.2343A>T
ENST00000680742.1:c.2426A>T ENSP00000505206.1:p.Gln809Leu
ENST00000680885.1:n.2347A>T
ENST00000681158.1:c.2215A>T
ENST00000681173.1:n.2215A>T
ENST00000681203.1:c.2354A>T ENSP00000506456.1:p.Gln785Leu
ENST00000681425.1:n.2347A>T
ENST00000328194.7:c.2426A>T ENSP00000328524.3:p.Gln809Leu
ENST00000526707.5:c.2354A>T ENSP00000436780.1:p.Gln785Leu
ENST00000527700.5:n.1988A>T
ENST00000530044.5:c.2426A>T ENSP00000435866.1:p.Gln809Leu
NM_001243254.1:c.2426A>T NP_001230183.1:p.Gln809Leu
NM_015213.3:c.2426A>T NP_056028.2:p.Gln809Leu
XM_005252832.1:c.2426A>T XP_005252889.1:p.Gln809Leu
XM_011519952.1:c.2426A>T XP_011518254.1:p.Gln809Leu
XM_011519953.1:c.524A>T XP_011518255.1:p.Gln175Leu
XR_242782.2:n.2691A>T
XR_930851.1:n.2691A>T
XR_930852.1:n.2691A>T
XR_930853.1:n.2540A>T
NM_001348749.1:c.2354A>T NP_001335678.1:p.Gln785Leu
NM_001348750.1:c.2138A>T NP_001335679.1:p.Gln713Leu
NR_145966.2:n.2683A>T
NM_015213.4:c.2426A>T MANE Select NP_056028.2:p.Gln809Leu
NM_001243254.2:c.2426A>T NP_001230183.1:p.Gln809Leu
NM_001348749.2:c.2354A>T NP_001335678.1:p.Gln785Leu
NM_001348750.2:c.2138A>T NP_001335679.1:p.Gln713Leu