Canonical Allele Identifier: CA645597934
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034171_28034172insGGCCTTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGC , CM000675.2:g.28034171_28034172insGGCCTTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGC GRCh38
NC_000013.10:g.28608308_28608309insGGCCTTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGC , CM000675.1:g.28608308_28608309insGGCCTTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGC GRCh37
NC_000013.9:g.27506308_27506309insGGCCTTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGC NCBI36
NG_007066.1:g.71444_71445insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA , LRG_457:g.71444_71445insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA MANE Select ENSP00000241453.7:p.Glu598_Tyr599insGlyArgSerSerAspAsnGluTyrP...
ENST00000241453.11:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA ENSP00000241453.7:p.Glu598_Tyr599insGlyArgSerSerAspAsnGluTyrP...
ENST00000380987.2:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA ENSP00000370374.2:p.Glu598_Tyr599insGlyArgSerSerAspAsnGluTyrP...
NM_004119.2:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA , LRG_457t1:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA NP_004110.2:p.Glu598_Tyr599insGlyArgSerSerAspAsnGluTyrPheTyrV...
NR_130706.1:n.1876_1877insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA
XM_011535015.1:c.1737_1738insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533317.1:p.Glu579_Tyr580insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535016.1:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533318.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535017.1:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533319.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535018.1:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533320.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535015.2:c.1737_1738insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533317.1:p.Glu579_Tyr580insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535017.2:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533319.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_011535018.2:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_011533320.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_017020486.1:c.1578_1579insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_016875975.1:p.Glu526_Tyr527insGlyArgSerSerAspAsnGluTyrPheT...
XM_017020487.1:c.1269_1270insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_016875976.1:p.Glu423_Tyr424insGlyArgSerSerAspAsnGluTyrPheT...
XM_017020488.1:c.915_916insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_016875977.1:p.Glu305_Tyr306insGlyArgSerSerAspAsnGluTyrPheT...
XM_017020489.1:c.897_898insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA XP_016875978.1:p.Glu299_Tyr300insGlyArgSerSerAspAsnGluTyrPheT...
NM_004119.3:c.1794_1795insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA MANE Select NP_004110.2:p.Glu598_Tyr599insGlyArgSerSerAspAsnGluTyrPheTyrV...
NR_130706.2:n.1860_1861insGGCCGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAA