Canonical Allele Identifier: CA2573332296
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018491_28018492insCCA , CM000675.2:g.28018491_28018492insCCA GRCh38
NC_000013.10:g.28592628_28592629insCCA , CM000675.1:g.28592628_28592629insCCA GRCh37
NC_000013.9:g.27490628_27490629insCCA NCBI36
NG_007066.1:g.87078_87079insGGT , LRG_457:g.87078_87079insGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2517_2518insGGT MANE Select ENSP00000241453.7:p.Asp839_Ser840insGly
ENST00000241453.11:c.2517_2518insGGT ENSP00000241453.7:p.Asp839_Ser840insGly
ENST00000380987.2:c.*429_*430insGGT ENSP00000370374.2:n.*429_*430insGGT
NM_004119.2:c.2517_2518insGGT , LRG_457t1:c.2517_2518insGGT NP_004110.2:p.Asp839_Ser840insGly
NR_130706.1:n.2731_2732insGGT
XM_011535015.1:c.2460_2461insGGT XP_011533317.1:p.Asp820_Ser821insGly
XM_011535016.1:c.1992_1993insGGT XP_011533318.1:p.Asp664_Ser665insGly
XM_011535017.1:c.1992_1993insGGT XP_011533319.1:p.Asp664_Ser665insGly
XM_011535018.1:c.1992_1993insGGT XP_011533320.1:p.Asp664_Ser665insGly
XM_011535015.2:c.2460_2461insGGT XP_011533317.1:p.Asp820_Ser821insGly
XM_011535017.2:c.1992_1993insGGT XP_011533319.1:p.Asp664_Ser665insGly
XM_011535018.2:c.1992_1993insGGT XP_011533320.1:p.Asp664_Ser665insGly
XM_017020486.1:c.2301_2302insGGT XP_016875975.1:p.Asp767_Ser768insGly
XM_017020487.1:c.1992_1993insGGT XP_016875976.1:p.Asp664_Ser665insGly
XM_017020488.1:c.1638_1639insGGT XP_016875977.1:p.Asp546_Ser547insGly
XM_017020489.1:c.1620_1621insGGT XP_016875978.1:p.Asp540_Ser541insGly
NM_004119.3:c.2517_2518insGGT MANE Select NP_004110.2:p.Asp839_Ser840insGly
NR_130706.2:n.2715_2716insGGT