Canonical Allele Identifier: CA645597752
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034153_28034154insTCTCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGT , CM000675.2:g.28034153_28034154insTCTCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGT GRCh38
NC_000013.10:g.28608290_28608291insTCTCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGT , CM000675.1:g.28608290_28608291insTCTCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGT GRCh37
NC_000013.9:g.27506290_27506291insTCTCAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGT NCBI36
NG_007066.1:g.71487_71488insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457:g.71487_71488insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select ENSP00000241453.7:p.Phe612_Gly613insGluAsnPheTyrValAspPheArgG...
ENST00000241453.11:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG ENSP00000241453.7:p.Phe612_Gly613insGluAsnPheTyrValAspPheArgG...
ENST00000380987.2:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG ENSP00000370374.2:p.Phe612_Gly613insGluAsnPheTyrValAspPheArgG...
NM_004119.2:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457t1:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG NP_004110.2:p.Phe612_Gly613insGluAsnPheTyrValAspPheArgGluTyrG...
NR_130706.1:n.1919_1919+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG
XM_011535015.1:c.1780_1780+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533317.1:p.Phe593_Gly594insGluAsnPheTyrValAspPheArgGluT...
XM_011535016.1:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533318.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_011535017.1:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533319.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_011535018.1:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533320.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_011535015.2:c.1780_1780+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533317.1:p.Phe593_Gly594insGluAsnPheTyrValAspPheArgGluT...
XM_011535017.2:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533319.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_011535018.2:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_011533320.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_017020486.1:c.1621_1621+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875975.1:p.Phe540_Gly541insGluAsnPheTyrValAspPheArgGluT...
XM_017020487.1:c.1312_1312+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875976.1:p.Phe437_Gly438insGluAsnPheTyrValAspPheArgGluT...
XM_017020488.1:c.958_958+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875977.1:p.Phe319_Gly320insGluAsnPheTyrValAspPheArgGluT...
XM_017020489.1:c.940_940+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG XP_016875978.1:p.Phe313_Gly314insGluAsnPheTyrValAspPheArgGluT...
NM_004119.3:c.1837_1837+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select NP_004110.2:p.Phe612_Gly613insGluAsnPheTyrValAspPheArgGluTyrG...
NR_130706.2:n.1903_1903+1insAGAACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG