Canonical Allele Identifier: CA472333965

Gene: DEAF1

Linked Data

• MyVariant Identifiers: chr11:g.686981G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.686981G>A , CM000673.2:g.686981G>A	GRCh38
NC_000011.9:g.686981G>A , CM000673.1:g.686981G>A	GRCh37
NC_000011.8:g.676981G>A	NCBI36
NG_034156.1:g.13774C>T
NG_034156.2:g.25103C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525626.6:n.566C>T
ENST00000528864.6:n.567C>T
ENST00000529717.6:c.*386C>T	ENSP00000432518.2:n.*386C>T
ENST00000530813.2:c.*304C>T	ENSP00000508507.1:n.*304C>T
ENST00000682936.1:n.441C>T
ENST00000683307.1:c.-46C>T	ENSP00000507198.1:n.-46C>T
ENST00000684249.1:n.869C>T
ENST00000685854.1:c.477C>T	ENSP00000508801.1:p.Cys159=
ENST00000686001.1:c.477C>T	ENSP00000508459.1:p.Cys159=
ENST00000687329.1:c.477C>T	ENSP00000510598.1:p.Cys159=
ENST00000689835.1:c.477C>T	ENSP00000510621.1:p.Cys159=
ENST00000690068.1:c.477C>T	ENSP00000509089.1:p.Cys159=
ENST00000692634.1:c.477C>T	ENSP00000508859.1:p.Cys159=
ENST00000693164.1:n.675C>T
ENST00000382409.4:c.681C>T MANE Select	ENSP00000371846.3:p.Cys227=
ENST00000382409.3:c.681C>T	ENSP00000371846.3:p.Cys227=
ENST00000525626.5:n.536C>T
ENST00000527170.5:c.43C>T
ENST00000528864.5:n.548C>T
ENST00000529717.5:c.645C>T
NM_001293634.1:c.664+930C>T	NP_001280563.1:n.664+930C>T
NM_021008.3:c.681C>T	NP_066288.2:p.Cys227=
XM_011519842.1:c.681C>T	XP_011518144.1:p.Cys227=
XM_011519843.1:c.681C>T	XP_011518145.1:p.Cys227=
XR_428838.2:n.687C>T
XR_930843.1:n.687C>T
XM_011519842.3:c.681C>T	XP_011518144.1:p.Cys227=
XM_024448325.1:c.681C>T	XP_024304093.1:p.Cys227=
XM_024448326.1:c.681C>T	XP_024304094.1:p.Cys227=
XM_024448327.1:c.681C>T	XP_024304095.1:p.Cys227=
NM_001367390.1:c.-46C>T	NP_001354319.1:n.-46C>T
NM_021008.4:c.681C>T MANE Select	NP_066288.2:p.Cys227=