Canonical Allele Identifier: CA378932716

Gene: DEAF1

Linked Data

• MyVariant Identifiers: chr11:g.686967T>A (hg19) ; chr11:g.686967T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.686967T>A , CM000673.2:g.686967T>A	GRCh38
NC_000011.9:g.686967T>A , CM000673.1:g.686967T>A	GRCh37
NC_000011.8:g.676967T>A	NCBI36
NG_034156.1:g.13788A>T
NG_034156.2:g.25117A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525626.6:n.580A>T
ENST00000528864.6:n.581A>T
ENST00000529717.6:c.*400A>T	ENSP00000432518.2:n.*400A>T
ENST00000530813.2:c.*318A>T	ENSP00000508507.1:n.*318A>T
ENST00000682936.1:n.455A>T
ENST00000683307.1:c.-32A>T	ENSP00000507198.1:n.-32A>T
ENST00000684249.1:n.883A>T
ENST00000685854.1:c.491A>T	ENSP00000508801.1:p.Glu164Val
ENST00000686001.1:c.491A>T	ENSP00000508459.1:p.Glu164Val
ENST00000687329.1:c.491A>T	ENSP00000510598.1:p.Glu164Val
ENST00000689835.1:c.491A>T	ENSP00000510621.1:p.Glu164Val
ENST00000690068.1:c.491A>T	ENSP00000509089.1:p.Glu164Val
ENST00000692634.1:c.491A>T	ENSP00000508859.1:p.Glu164Val
ENST00000693164.1:n.689A>T
ENST00000382409.4:c.695A>T MANE Select	ENSP00000371846.3:p.Glu232Val
ENST00000382409.3:c.695A>T	ENSP00000371846.3:p.Glu232Val
ENST00000525626.5:n.550A>T
ENST00000527170.5:c.57A>T
ENST00000529717.5:c.659A>T
NM_001293634.1:c.664+944A>T	NP_001280563.1:n.664+944A>T
NM_021008.3:c.695A>T	NP_066288.2:p.Glu232Val
XM_011519842.1:c.695A>T	XP_011518144.1:p.Glu232Val
XM_011519843.1:c.695A>T	XP_011518145.1:p.Glu232Val
XR_428838.2:n.701A>T
XR_930843.1:n.701A>T
XM_011519842.3:c.695A>T	XP_011518144.1:p.Glu232Val
XM_024448325.1:c.695A>T	XP_024304093.1:p.Glu232Val
XM_024448326.1:c.695A>T	XP_024304094.1:p.Glu232Val
XM_024448327.1:c.695A>T	XP_024304095.1:p.Glu232Val
NM_001367390.1:c.-32A>T	NP_001354319.1:n.-32A>T
NM_021008.4:c.695A>T MANE Select	NP_066288.2:p.Glu232Val