Canonical Allele Identifier: CA891842154
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034124_28034125insAAAATCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATA , CM000675.2:g.28034124_28034125insAAAATCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATA GRCh38
NC_000013.10:g.28608261_28608262insAAAATCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATA , CM000675.1:g.28608261_28608262insAAAATCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATA GRCh37
NC_000013.9:g.27506261_27506262insAAAATCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATA NCBI36
NG_007066.1:g.71487_71488insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457:g.71487_71488insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select ENSP00000241453.7:p.Phe612_Gly613insAspPheTyrAspLeuLysTrpGluP...
ENST00000241453.11:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG ENSP00000241453.7:p.Phe612_Gly613insAspPheTyrAspLeuLysTrpGluP...
ENST00000380987.2:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG ENSP00000370374.2:p.Phe612_Gly613insAspPheTyrAspLeuLysTrpGluP...
NM_004119.2:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457t1:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG NP_004110.2:p.Phe612_Gly613insAspPheTyrAspLeuLysTrpGluPheProA...
NR_130706.1:n.1919_1919+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG
XM_011535015.1:c.1780_1780+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533317.1:p.Phe593_Gly594insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535016.1:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533318.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535017.1:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533319.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535018.1:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533320.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535015.2:c.1780_1780+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533317.1:p.Phe593_Gly594insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535017.2:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533319.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_011535018.2:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533320.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_017020486.1:c.1621_1621+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875975.1:p.Phe540_Gly541insAspPheTyrAspLeuLysTrpGluPheP...
XM_017020487.1:c.1312_1312+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875976.1:p.Phe437_Gly438insAspPheTyrAspLeuLysTrpGluPheP...
XM_017020488.1:c.958_958+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875977.1:p.Phe319_Gly320insAspPheTyrAspLeuLysTrpGluPheP...
XM_017020489.1:c.940_940+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875978.1:p.Phe313_Gly314insAspPheTyrAspLeuLysTrpGluPheP...
NM_004119.3:c.1837_1837+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select NP_004110.2:p.Phe612_Gly613insAspPheTyrAspLeuLysTrpGluPheProA...
NR_130706.2:n.1903_1903+1insATTTTTATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG