Canonical Allele Identifier: CA1947253031
Gene: DEAF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.686897G= , CM000673.2:g.686897G= GRCh38
NC_000011.9:g.686897G= , CM000673.1:g.686897G= GRCh37
NC_000011.8:g.676897G= NCBI36
NG_034156.1:g.13858C=
NG_034156.2:g.25187C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525626.6:n.650C=
ENST00000528864.6:n.651C=
ENST00000530813.2:c.*388C= ENSP00000508507.1:n.*388C=
ENST00000682936.1:n.525C=
ENST00000683307.1:c.39C= ENSP00000507198.1:p.Ser13=
ENST00000684249.1:n.953C=
ENST00000685854.1:c.561C= ENSP00000508801.1:p.Ser187=
ENST00000686001.1:c.561C= ENSP00000508459.1:p.Ser187=
ENST00000687329.1:c.561C= ENSP00000510598.1:p.Ser187=
ENST00000689835.1:c.561C= ENSP00000510621.1:p.Ser187=
ENST00000690068.1:c.561C= ENSP00000509089.1:p.Ser187=
ENST00000692634.1:c.561C= ENSP00000508859.1:p.Ser187=
ENST00000693164.1:n.759C=
ENST00000382409.4:c.765C= MANE Select ENSP00000371846.3:p.Ser255=
ENST00000382409.3:c.765C= ENSP00000371846.3:p.Ser255=
ENST00000527170.5:c.127C=
NM_001293634.1:c.664+1014C= NP_001280563.1:n.664+1014C=
NM_021008.3:c.765C= NP_066288.2:p.Ser255=
XM_011519842.1:c.765C= XP_011518144.1:p.Ser255=
XM_011519843.1:c.765C= XP_011518145.1:p.Ser255=
XR_428838.2:n.771C=
XR_930843.1:n.771C=
XM_011519842.3:c.765C= XP_011518144.1:p.Ser255=
XM_024448325.1:c.765C= XP_024304093.1:p.Ser255=
XM_024448326.1:c.765C= XP_024304094.1:p.Ser255=
XM_024448327.1:c.765C= XP_024304095.1:p.Ser255=
NM_001367390.1:c.39C= NP_001354319.1:p.Ser13=
NM_021008.4:c.765C= MANE Select NP_066288.2:p.Ser255=