Canonical Allele Identifier: CA645597775

Gene: FLT3

Linked Data

• COSMIC: COSM250175 ; COSM256016

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034149_28034150insGGTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAG , CM000675.2:g.28034149_28034150insGGTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAG	GRCh38
NC_000013.10:g.28608286_28608287insGGTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAG , CM000675.1:g.28608286_28608287insGGTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAG	GRCh37
NC_000013.9:g.27506286_27506287insGGTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAG	NCBI36
NG_007066.1:g.71480_71481insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA , LRG_457:g.71480_71481insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA MANE Select	ENSP00000241453.7:p.Leu610_Glu611insProTyrValAspPheArgGluTyrG...
ENST00000241453.11:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	ENSP00000241453.7:p.Leu610_Glu611insProTyrValAspPheArgGluTyrG...
ENST00000380987.2:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	ENSP00000370374.2:p.Leu610_Glu611insProTyrValAspPheArgGluTyrG...
NM_004119.2:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA , LRG_457t1:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	NP_004110.2:p.Leu610_Glu611insProTyrValAspPheArgGluTyrGluTyrA...
NR_130706.1:n.1912_1913insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA
XM_011535015.1:c.1773_1774insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533317.1:p.Leu591_Glu592insProTyrValAspPheArgGluTyrGluT...
XM_011535016.1:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533318.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_011535017.1:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533319.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_011535018.1:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533320.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_011535015.2:c.1773_1774insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533317.1:p.Leu591_Glu592insProTyrValAspPheArgGluTyrGluT...
XM_011535017.2:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533319.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_011535018.2:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_011533320.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_017020486.1:c.1614_1615insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_016875975.1:p.Leu538_Glu539insProTyrValAspPheArgGluTyrGluT...
XM_017020487.1:c.1305_1306insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_016875976.1:p.Leu435_Glu436insProTyrValAspPheArgGluTyrGluT...
XM_017020488.1:c.951_952insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_016875977.1:p.Leu317_Glu318insProTyrValAspPheArgGluTyrGluT...
XM_017020489.1:c.933_934insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA	XP_016875978.1:p.Leu311_Glu312insProTyrValAspPheArgGluTyrGluT...
NM_004119.3:c.1830_1831insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA MANE Select	NP_004110.2:p.Leu610_Glu611insProTyrValAspPheArgGluTyrGluTyrA...
NR_130706.2:n.1896_1897insCCCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTA