Canonical Allele Identifier: CA645597928

Gene: FLT3

Linked Data

• COSMIC: COSM5351705

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034179_28034180insCATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACC , CM000675.2:g.28034179_28034180insCATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACC	GRCh38
NC_000013.10:g.28608316_28608317insCATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACC , CM000675.1:g.28608316_28608317insCATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACC	GRCh37
NC_000013.9:g.27506316_27506317insCATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACC	NCBI36
NG_007066.1:g.71445_71446insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT , LRG_457:g.71445_71446insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT MANE Select	ENSP00000241453.7:p.Glu598_Tyr599insTrpValThrGlySerSerAspAsnG...
ENST00000241453.11:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	ENSP00000241453.7:p.Glu598_Tyr599insTrpValThrGlySerSerAspAsnG...
ENST00000380987.2:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	ENSP00000370374.2:p.Glu598_Tyr599insTrpValThrGlySerSerAspAsnG...
NM_004119.2:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT , LRG_457t1:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	NP_004110.2:p.Glu598_Tyr599insTrpValThrGlySerSerAspAsnGluTyrP...
NR_130706.1:n.1877_1878insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT
XM_011535015.1:c.1738_1739insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533317.1:p.Glu579_Tyr580insTrpValThrGlySerSerAspAsnGluT...
XM_011535016.1:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533318.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_011535017.1:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533319.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_011535018.1:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533320.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_011535015.2:c.1738_1739insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533317.1:p.Glu579_Tyr580insTrpValThrGlySerSerAspAsnGluT...
XM_011535017.2:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533319.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_011535018.2:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_011533320.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_017020486.1:c.1579_1580insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_016875975.1:p.Glu526_Tyr527insTrpValThrGlySerSerAspAsnGluT...
XM_017020487.1:c.1270_1271insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_016875976.1:p.Glu423_Tyr424insTrpValThrGlySerSerAspAsnGluT...
XM_017020488.1:c.916_917insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_016875977.1:p.Glu305_Tyr306insTrpValThrGlySerSerAspAsnGluT...
XM_017020489.1:c.898_899insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT	XP_016875978.1:p.Glu299_Tyr300insTrpValThrGlySerSerAspAsnGluT...
NM_004119.3:c.1795_1796insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT MANE Select	NP_004110.2:p.Glu598_Tyr599insTrpValThrGlySerSerAspAsnGluTyrP...
NR_130706.2:n.1861_1862insGGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT