Canonical Allele Identifier: CA645597967
Gene: FLT3 HGNC NCBI

Linked Data

COSMIC: COSM256021

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034131_28034157dup , CM000675.2:g.28034131_28034157dup GRCh38
NC_000013.10:g.28608268_28608294dup , CM000675.1:g.28608268_28608294dup GRCh37
NC_000013.9:g.27506268_27506294dup NCBI36
NG_007066.1:g.71412_71438dup , LRG_457:g.71412_71438dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1762_1788dup MANE Select ENSP00000241453.7:p.Glu596_Tyr597insGluTyrPheTyrValAspPheArgG...
ENST00000241453.11:c.1762_1788dup ENSP00000241453.7:p.Glu596_Tyr597insGluTyrPheTyrValAspPheArgG...
ENST00000380987.2:c.1762_1788dup ENSP00000370374.2:p.Glu596_Tyr597insGluTyrPheTyrValAspPheArgG...
NM_004119.2:c.1762_1788dup , LRG_457t1:c.1762_1788dup NP_004110.2:p.Glu596_Tyr597insGluTyrPheTyrValAspPheArgGlu
NR_130706.1:n.1844_1870dup
XM_011535015.1:c.1705_1731dup XP_011533317.1:p.Glu577_Tyr578insGluTyrPheTyrValAspPheArgGlu
XM_011535016.1:c.1237_1263dup XP_011533318.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_011535017.1:c.1237_1263dup XP_011533319.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_011535018.1:c.1237_1263dup XP_011533320.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_011535015.2:c.1705_1731dup XP_011533317.1:p.Glu577_Tyr578insGluTyrPheTyrValAspPheArgGlu
XM_011535017.2:c.1237_1263dup XP_011533319.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_011535018.2:c.1237_1263dup XP_011533320.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_017020486.1:c.1546_1572dup XP_016875975.1:p.Glu524_Tyr525insGluTyrPheTyrValAspPheArgGlu
XM_017020487.1:c.1237_1263dup XP_016875976.1:p.Glu421_Tyr422insGluTyrPheTyrValAspPheArgGlu
XM_017020488.1:c.883_909dup XP_016875977.1:p.Glu303_Tyr304insGluTyrPheTyrValAspPheArgGlu
XM_017020489.1:c.865_891dup XP_016875978.1:p.Glu297_Tyr298insGluTyrPheTyrValAspPheArgGlu
NM_004119.3:c.1762_1788dup MANE Select NP_004110.2:p.Glu596_Tyr597insGluTyrPheTyrValAspPheArgGlu
NR_130706.2:n.1828_1854dup