Canonical Allele Identifier: CA645597927
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034164_28034165insAGGGATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCT , CM000675.2:g.28034164_28034165insAGGGATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCT GRCh38
NC_000013.10:g.28608301_28608302insAGGGATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCT , CM000675.1:g.28608301_28608302insAGGGATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCT GRCh37
NC_000013.9:g.27506301_27506302insAGGGATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCT NCBI36
NG_007066.1:g.71445_71446insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT , LRG_457:g.71445_71446insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT MANE Select ENSP00000241453.7:p.Glu598_Tyr599insSerLeuAspAsnGluTyrPheTyrV...
ENST00000241453.11:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT ENSP00000241453.7:p.Glu598_Tyr599insSerLeuAspAsnGluTyrPheTyrV...
ENST00000380987.2:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT ENSP00000370374.2:p.Glu598_Tyr599insSerLeuAspAsnGluTyrPheTyrV...
NM_004119.2:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT , LRG_457t1:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT NP_004110.2:p.Glu598_Tyr599insSerLeuAspAsnGluTyrPheTyrValAspP...
NR_130706.1:n.1877_1878insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT
XM_011535015.1:c.1738_1739insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533317.1:p.Glu579_Tyr580insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535016.1:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533318.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535017.1:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533319.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535018.1:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533320.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535015.2:c.1738_1739insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533317.1:p.Glu579_Tyr580insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535017.2:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533319.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_011535018.2:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_011533320.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_017020486.1:c.1579_1580insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_016875975.1:p.Glu526_Tyr527insSerLeuAspAsnGluTyrPheTyrValA...
XM_017020487.1:c.1270_1271insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_016875976.1:p.Glu423_Tyr424insSerLeuAspAsnGluTyrPheTyrValA...
XM_017020488.1:c.916_917insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_016875977.1:p.Glu305_Tyr306insSerLeuAspAsnGluTyrPheTyrValA...
XM_017020489.1:c.898_899insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT XP_016875978.1:p.Glu299_Tyr300insSerLeuAspAsnGluTyrPheTyrValA...
NM_004119.3:c.1795_1796insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT MANE Select NP_004110.2:p.Glu598_Tyr599insSerLeuAspAsnGluTyrPheTyrValAspP...
NR_130706.2:n.1861_1862insCCCTAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAAT