Canonical Allele Identifier: CA645597757
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034152_28034153insCCCTGAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAG , CM000675.2:g.28034152_28034153insCCCTGAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAG GRCh38
NC_000013.10:g.28608289_28608290insCCCTGAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAG , CM000675.1:g.28608289_28608290insCCCTGAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAG GRCh37
NC_000013.9:g.27506289_27506290insCCCTGAAACTCTAAATTTTCTCTTGGAAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAG NCBI36
NG_007066.1:g.71486_71487insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT , LRG_457:g.71486_71487insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT MANE Select ENSP00000241453.7:p.Phe612_Gly613insGlnGlyPheTyrValAspPheArgG...
ENST00000241453.11:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT ENSP00000241453.7:p.Phe612_Gly613insGlnGlyPheTyrValAspPheArgG...
ENST00000380987.2:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT ENSP00000370374.2:p.Phe612_Gly613insGlnGlyPheTyrValAspPheArgG...
NM_004119.2:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT , LRG_457t1:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT NP_004110.2:p.Phe612_Gly613insGlnGlyPheTyrValAspPheArgGluTyrG...
NR_130706.1:n.1918_1919insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT
XM_011535015.1:c.1779_1780insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533317.1:p.Phe593_Gly594insGlnGlyPheTyrValAspPheArgGluT...
XM_011535016.1:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533318.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_011535017.1:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533319.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_011535018.1:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533320.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_011535015.2:c.1779_1780insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533317.1:p.Phe593_Gly594insGlnGlyPheTyrValAspPheArgGluT...
XM_011535017.2:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533319.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_011535018.2:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_011533320.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_017020486.1:c.1620_1621insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_016875975.1:p.Phe540_Gly541insGlnGlyPheTyrValAspPheArgGluT...
XM_017020487.1:c.1311_1312insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_016875976.1:p.Phe437_Gly438insGlnGlyPheTyrValAspPheArgGluT...
XM_017020488.1:c.957_958insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_016875977.1:p.Phe319_Gly320insGlnGlyPheTyrValAspPheArgGluT...
XM_017020489.1:c.939_940insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT XP_016875978.1:p.Phe313_Gly314insGlnGlyPheTyrValAspPheArgGluT...
NM_004119.3:c.1836_1837insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT MANE Select NP_004110.2:p.Phe612_Gly613insGlnGlyPheTyrValAspPheArgGluTyrG...
NR_130706.2:n.1902_1903insCAGGGCTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTT