Canonical Allele Identifier: CA645597863

Gene: FLT3

Linked Data

• COSMIC: COSM19882

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034165_28034166insGGTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTG , CM000675.2:g.28034165_28034166insGGTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTG	GRCh38
NC_000013.10:g.28608302_28608303insGGTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTG , CM000675.1:g.28608302_28608303insGGTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTG	GRCh37
NC_000013.9:g.27506302_27506303insGGTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTG	NCBI36
NG_007066.1:g.71455_71456insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA , LRG_457:g.71455_71456insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA MANE Select	ENSP00000241453.7:p.Leu601_Lys602insAsnProAspAsnGluTyrPheTyrV...
ENST00000241453.11:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	ENSP00000241453.7:p.Leu601_Lys602insAsnProAspAsnGluTyrPheTyrV...
ENST00000380987.2:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	ENSP00000370374.2:p.Leu601_Lys602insAsnProAspAsnGluTyrPheTyrV...
NM_004119.2:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA , LRG_457t1:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	NP_004110.2:p.Leu601_Lys602insAsnProAspAsnGluTyrPheTyrValAspP...
NR_130706.1:n.1887_1888insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA
XM_011535015.1:c.1748_1749insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533317.1:p.Leu582_Lys583insAsnProAspAsnGluTyrPheTyrValA...
XM_011535016.1:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533318.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_011535017.1:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533319.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_011535018.1:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533320.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_011535015.2:c.1748_1749insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533317.1:p.Leu582_Lys583insAsnProAspAsnGluTyrPheTyrValA...
XM_011535017.2:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533319.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_011535018.2:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_011533320.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_017020486.1:c.1589_1590insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_016875975.1:p.Leu529_Lys530insAsnProAspAsnGluTyrPheTyrValA...
XM_017020487.1:c.1280_1281insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_016875976.1:p.Leu426_Lys427insAsnProAspAsnGluTyrPheTyrValA...
XM_017020488.1:c.926_927insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_016875977.1:p.Leu308_Lys309insAsnProAspAsnGluTyrPheTyrValA...
XM_017020489.1:c.908_909insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA	XP_016875978.1:p.Leu302_Lys303insAsnProAspAsnGluTyrPheTyrValA...
NM_004119.3:c.1805_1806insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA MANE Select	NP_004110.2:p.Leu601_Lys602insAsnProAspAsnGluTyrPheTyrValAspP...
NR_130706.2:n.1871_1872insCCCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAA