Canonical Allele Identifier: CA379598059

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163616T>A (hg19) ; chr11:g.9142069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142069T>A , CM000673.2:g.9142069T>A	GRCh38
NC_000011.9:g.9163616T>A , CM000673.1:g.9163616T>A	GRCh37
NC_000011.8:g.9120192T>A	NCBI36
NG_053019.1:g.128267A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3551A>T MANE Select	ENSP00000328524.3:p.Glu1184Val
ENST00000525784.6:n.1413A>T
ENST00000530780.2:c.*3377A>T	ENSP00000433925.1:n.*3377A>T
ENST00000531747.2:n.3222A>T
ENST00000679446.1:n.3472A>T
ENST00000679458.1:n.4952A>T
ENST00000679460.1:n.4613A>T
ENST00000679568.1:c.3551A>T	ENSP00000505860.1:p.Glu1184Val
ENST00000679745.1:n.4056A>T
ENST00000679773.1:n.2712A>T
ENST00000679926.1:n.4853A>T
ENST00000679999.1:c.*608A>T	ENSP00000505198.1:n.*608A>T
ENST00000680252.1:c.3218A>T
ENST00000680294.1:c.3344A>T	ENSP00000506113.1:p.Glu1115Val
ENST00000680358.1:n.2850A>T
ENST00000680470.1:c.*1332A>T	ENSP00000505975.1:n.*1332A>T
ENST00000680554.1:c.*84A>T	ENSP00000505621.1:n.*84A>T
ENST00000680576.1:n.5027A>T
ENST00000680599.1:n.3592A>T
ENST00000680742.1:c.*84A>T	ENSP00000505206.1:n.*84A>T
ENST00000680791.1:n.2435A>T
ENST00000680885.1:n.5253A>T
ENST00000681158.1:c.3135A>T
ENST00000681203.1:c.3479A>T	ENSP00000506456.1:p.Glu1160Val
ENST00000681371.1:n.3423A>T
ENST00000681425.1:n.4029A>T
ENST00000681639.1:n.1830A>T
ENST00000328194.7:c.3551A>T	ENSP00000328524.3:p.Glu1184Val
ENST00000525784.5:c.487A>T
ENST00000527700.5:n.3113A>T
ENST00000528725.5:c.247A>T
ENST00000529977.5:n.1452A>T
ENST00000530044.5:c.3551A>T	ENSP00000435866.1:p.Glu1184Val
ENST00000531747.1:c.787A>T
ENST00000533737.5:c.214A>T
NM_001243254.1:c.3551A>T	NP_001230183.1:p.Glu1184Val
NM_015213.3:c.3551A>T	NP_056028.2:p.Glu1184Val
XM_005252832.1:c.3551A>T	XP_005252889.1:p.Glu1184Val
XM_011519952.1:c.3551A>T	XP_011518254.1:p.Glu1184Val
XM_011519953.1:c.1649A>T	XP_011518255.1:p.Glu550Val
XR_242782.2:n.3733A>T
XR_930851.1:n.3733A>T
NM_001348749.1:c.3479A>T	NP_001335678.1:p.Glu1160Val
NM_001348750.1:c.3263A>T	NP_001335679.1:p.Glu1088Val
NR_145966.2:n.3725A>T
NM_015213.4:c.3551A>T MANE Select	NP_056028.2:p.Glu1184Val
NM_001243254.2:c.3551A>T	NP_001230183.1:p.Glu1184Val
NM_001348749.2:c.3479A>T	NP_001335678.1:p.Glu1160Val
NM_001348750.2:c.3263A>T	NP_001335679.1:p.Glu1088Val