Canonical Allele Identifier: CA645597857
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034147_28034148insGGATCGATTTGAGATCATATTCATATTCTCTGAAATCAACGT , CM000675.2:g.28034147_28034148insGGATCGATTTGAGATCATATTCATATTCTCTGAAATCAACGT GRCh38
NC_000013.10:g.28608284_28608285insGGATCGATTTGAGATCATATTCATATTCTCTGAAATCAACGT , CM000675.1:g.28608284_28608285insGGATCGATTTGAGATCATATTCATATTCTCTGAAATCAACGT GRCh37
NC_000013.9:g.27506284_27506285insGGATCGATTTGAGATCATATTCATATTCTCTGAAATCAACGT NCBI36
NG_007066.1:g.71457_71458insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT , LRG_457:g.71457_71458insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT MANE Select ENSP00000241453.7:p.Lys602_Trp603insSerIleHisValAspPheArgGluT...
ENST00000241453.11:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT ENSP00000241453.7:p.Lys602_Trp603insSerIleHisValAspPheArgGluT...
ENST00000380987.2:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT ENSP00000370374.2:p.Lys602_Trp603insSerIleHisValAspPheArgGluT...
NM_004119.2:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT , LRG_457t1:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT NP_004110.2:p.Lys602_Trp603insSerIleHisValAspPheArgGluTyrGluT...
NR_130706.1:n.1889_1890insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT
XM_011535015.1:c.1750_1751insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533317.1:p.Lys583_Trp584insSerIleHisValAspPheArgGluTyrG...
XM_011535016.1:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533318.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_011535017.1:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533319.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_011535018.1:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533320.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_011535015.2:c.1750_1751insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533317.1:p.Lys583_Trp584insSerIleHisValAspPheArgGluTyrG...
XM_011535017.2:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533319.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_011535018.2:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_011533320.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_017020486.1:c.1591_1592insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_016875975.1:p.Lys530_Trp531insSerIleHisValAspPheArgGluTyrG...
XM_017020487.1:c.1282_1283insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_016875976.1:p.Lys427_Trp428insSerIleHisValAspPheArgGluTyrG...
XM_017020488.1:c.928_929insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_016875977.1:p.Lys309_Trp310insSerIleHisValAspPheArgGluTyrG...
XM_017020489.1:c.910_911insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT XP_016875978.1:p.Lys303_Trp304insSerIleHisValAspPheArgGluTyrG...
NM_004119.3:c.1807_1808insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT MANE Select NP_004110.2:p.Lys602_Trp603insSerIleHisValAspPheArgGluTyrGluT...
NR_130706.2:n.1873_1874insCGATCCACGTTGATTTCAGAGAATATGAATATGATCTCAAAT