Canonical Allele Identifier: CA645598045

Gene: FLT3

Linked Data

• COSMIC: COSM5879560

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034171_28034172insTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCGAAG , CM000675.2:g.28034171_28034172insTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCGAAG	GRCh38
NC_000013.10:g.28608308_28608309insTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCGAAG , CM000675.1:g.28608308_28608309insTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCGAAG	GRCh37
NC_000013.9:g.27506308_27506309insTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCCGGTCACCTGTACCATCTGTAGCTGGCTTTCGAAG	NCBI36
NG_007066.1:g.71397_71398insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA , LRG_457:g.71397_71398insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA MANE Select	ENSP00000241453.7:p.Gly583AlafsTer11
ENST00000241453.11:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	ENSP00000241453.7:p.Gly583AlafsTer11
ENST00000380987.2:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	ENSP00000370374.2:p.Gly583AlafsTer11
NM_004119.2:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA , LRG_457t1:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	NP_004110.2:p.Gly583AlafsTer11
NR_130706.1:n.1829_1830insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA
XM_011535015.1:c.1690_1691insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533317.1:p.Gly564AlafsTer11
XM_011535016.1:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533318.1:p.Gly408AlafsTer11
XM_011535017.1:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533319.1:p.Gly408AlafsTer11
XM_011535018.1:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533320.1:p.Gly408AlafsTer11
XM_011535015.2:c.1690_1691insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533317.1:p.Gly564AlafsTer11
XM_011535017.2:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533319.1:p.Gly408AlafsTer11
XM_011535018.2:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_011533320.1:p.Gly408AlafsTer11
XM_017020486.1:c.1531_1532insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_016875975.1:p.Gly511AlafsTer11
XM_017020487.1:c.1222_1223insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_016875976.1:p.Gly408AlafsTer11
XM_017020488.1:c.868_869insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_016875977.1:p.Gly290AlafsTer11
XM_017020489.1:c.850_851insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA	XP_016875978.1:p.Gly284AlafsTer11
NM_004119.3:c.1747_1748insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA MANE Select	NP_004110.2:p.Gly583AlafsTer11
NR_130706.2:n.1813_1814insCTTCGAAAGCCAGCTACAGATGGTACAGGTGACCGGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGA