Canonical Allele Identifier: CA2695202543
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034132_28034149dup , CM000675.2:g.28034132_28034149dup GRCh38
NC_000013.10:g.28608269_28608286dup , CM000675.1:g.28608269_28608286dup GRCh37
NC_000013.9:g.27506269_27506286dup NCBI36
NG_007066.1:g.71420_71437dup , LRG_457:g.71420_71437dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1770_1787dup MANE Select ENSP00000241453.7:p.Arg595_Glu596insAspTyrValAspPheArg
ENST00000241453.11:c.1770_1787dup ENSP00000241453.7:p.Arg595_Glu596insAspTyrValAspPheArg
ENST00000380987.2:c.1770_1787dup ENSP00000370374.2:p.Arg595_Glu596insAspTyrValAspPheArg
NM_004119.2:c.1770_1787dup , LRG_457t1:c.1770_1787dup NP_004110.2:p.Arg595_Glu596insAspTyrValAspPheArg
NR_130706.1:n.1852_1869dup
XM_011535015.1:c.1713_1730dup XP_011533317.1:p.Arg576_Glu577insAspTyrValAspPheArg
XM_011535016.1:c.1245_1262dup XP_011533318.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_011535017.1:c.1245_1262dup XP_011533319.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_011535018.1:c.1245_1262dup XP_011533320.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_011535015.2:c.1713_1730dup XP_011533317.1:p.Arg576_Glu577insAspTyrValAspPheArg
XM_011535017.2:c.1245_1262dup XP_011533319.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_011535018.2:c.1245_1262dup XP_011533320.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_017020486.1:c.1554_1571dup XP_016875975.1:p.Arg523_Glu524insAspTyrValAspPheArg
XM_017020487.1:c.1245_1262dup XP_016875976.1:p.Arg420_Glu421insAspTyrValAspPheArg
XM_017020488.1:c.891_908dup XP_016875977.1:p.Arg302_Glu303insAspTyrValAspPheArg
XM_017020489.1:c.873_890dup XP_016875978.1:p.Arg296_Glu297insAspTyrValAspPheArg
NM_004119.3:c.1770_1787dup MANE Select NP_004110.2:p.Arg595_Glu596insAspTyrValAspPheArg
NR_130706.2:n.1836_1853dup