Canonical Allele Identifier: CA2840601443

Gene: DEAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.686900dup , CM000673.2:g.686900dup	GRCh38
NC_000011.9:g.686900dup , CM000673.1:g.686900dup	GRCh37
NC_000011.8:g.676900dup	NCBI36
NG_034156.1:g.13856dup
NG_034156.2:g.25185dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525626.6:n.648dup
ENST00000528864.6:n.649dup
ENST00000530813.2:c.*386dup	ENSP00000508507.1:n.*386dup
ENST00000682936.1:n.523dup
ENST00000683307.1:c.37dup	ENSP00000507198.1:p.Ser13LysfsTer?
ENST00000684249.1:n.951dup
ENST00000685854.1:c.559dup	ENSP00000508801.1:p.Ser187LysfsTer?
ENST00000686001.1:c.559dup	ENSP00000508459.1:p.Ser187LysfsTer?
ENST00000687329.1:c.559dup	ENSP00000510598.1:p.Ser187LysfsTer?
ENST00000689835.1:c.559dup	ENSP00000510621.1:p.Ser187LysfsTer?
ENST00000690068.1:c.559dup	ENSP00000509089.1:p.Ser187LysfsTer?
ENST00000692634.1:c.559dup	ENSP00000508859.1:p.Ser187LysfsTer?
ENST00000693164.1:n.757dup
ENST00000382409.4:c.763dup MANE Select	ENSP00000371846.3:p.Ser255LysfsTer?
ENST00000382409.3:c.763dup	ENSP00000371846.3:p.Ser255LysfsTer?
ENST00000527170.5:c.125dup
NM_001293634.1:c.664+1012dup	NP_001280563.1:n.664+1012dup
NM_021008.3:c.763dup	NP_066288.2:p.Ser255LysfsTer?
XM_011519842.1:c.763dup	XP_011518144.1:p.Ser255LysfsTer?
XM_011519843.1:c.763dup	XP_011518145.1:p.Ser255LysfsTer?
XR_428838.2:n.769dup
XR_930843.1:n.769dup
XM_011519842.3:c.763dup	XP_011518144.1:p.Ser255LysfsTer?
XM_024448325.1:c.763dup	XP_024304093.1:p.Ser255LysfsTer?
XM_024448326.1:c.763dup	XP_024304094.1:p.Ser255LysfsTer?
XM_024448327.1:c.763dup	XP_024304095.1:p.Ser255LysfsTer?
NM_001367390.1:c.37dup	NP_001354319.1:p.Ser13LysfsTer?
NM_021008.4:c.763dup MANE Select	NP_066288.2:p.Ser255LysfsTer?