Canonical Allele Identifier: CA645597723

Gene: FLT3

Linked Data

• COSMIC: COSM5879399

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034129_28034130insGGGGTTCTTCTTTACCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCAT , CM000675.2:g.28034129_28034130insGGGGTTCTTCTTTACCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCAT	GRCh38
NC_000013.10:g.28608266_28608267insGGGGTTCTTCTTTACCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCAT , CM000675.1:g.28608266_28608267insGGGGTTCTTCTTTACCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCAT	GRCh37
NC_000013.9:g.27506266_27506267insGGGGTTCTTCTTTACCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCAT	NCBI36
NG_007066.1:g.71491_71492insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA , LRG_457:g.71491_71492insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
ENST00000241453.11:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
ENST00000380987.2:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
NM_004119.2:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA , LRG_457t1:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
NR_130706.1:n.1919+4_1919+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535015.1:c.1780+4_1780+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535016.1:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535017.1:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535018.1:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535015.2:c.1780+4_1780+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535017.2:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_011535018.2:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_017020486.1:c.1621+4_1621+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_017020487.1:c.1312+4_1312+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_017020488.1:c.958+4_958+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
XM_017020489.1:c.940+4_940+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
NM_004119.3:c.1837+4_1837+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA
NR_130706.2:n.1903+4_1903+5insAGAAGAACCCCATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTGGTAA