Canonical Allele Identifier: CA378932051
Gene: DEAF1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.686899T>A , CM000673.2:g.686899T>A GRCh38
NC_000011.9:g.686899T>A , CM000673.1:g.686899T>A GRCh37
NC_000011.8:g.676899T>A NCBI36
NG_034156.1:g.13856A>T
NG_034156.2:g.25185A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000525626.6:n.648A>T
ENST00000528864.6:n.649A>T
ENST00000530813.2:c.*386A>T ENSP00000508507.1:n.*386A>T
ENST00000682936.1:n.523A>T
ENST00000683307.1:c.37A>T ENSP00000507198.1:p.Ser13Cys
ENST00000684249.1:n.951A>T
ENST00000685854.1:c.559A>T ENSP00000508801.1:p.Ser187Cys
ENST00000686001.1:c.559A>T ENSP00000508459.1:p.Ser187Cys
ENST00000687329.1:c.559A>T ENSP00000510598.1:p.Ser187Cys
ENST00000689835.1:c.559A>T ENSP00000510621.1:p.Ser187Cys
ENST00000690068.1:c.559A>T ENSP00000509089.1:p.Ser187Cys
ENST00000692634.1:c.559A>T ENSP00000508859.1:p.Ser187Cys
ENST00000693164.1:n.757A>T
ENST00000382409.4:c.763A>T MANE Select ENSP00000371846.3:p.Ser255Cys
ENST00000382409.3:c.763A>T ENSP00000371846.3:p.Ser255Cys
ENST00000527170.5:c.125A>T
NM_001293634.1:c.664+1012A>T NP_001280563.1:n.664+1012A>T
NM_021008.3:c.763A>T NP_066288.2:p.Ser255Cys
XM_011519842.1:c.763A>T XP_011518144.1:p.Ser255Cys
XM_011519843.1:c.763A>T XP_011518145.1:p.Ser255Cys
XR_428838.2:n.769A>T
XR_930843.1:n.769A>T
XM_011519842.3:c.763A>T XP_011518144.1:p.Ser255Cys
XM_024448325.1:c.763A>T XP_024304093.1:p.Ser255Cys
XM_024448326.1:c.763A>T XP_024304094.1:p.Ser255Cys
XM_024448327.1:c.763A>T XP_024304095.1:p.Ser255Cys
NM_001367390.1:c.37A>T NP_001354319.1:p.Ser13Cys
NM_021008.4:c.763A>T MANE Select NP_066288.2:p.Ser255Cys