Canonical Allele Identifier: CA2798611854
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018833_28018834insTCTGCTCCTCTTTGGCCTCT , CM000675.2:g.28018833_28018834insTCTGCTCCTCTTTGGCCTCT GRCh38
NC_000013.10:g.28592970_28592971insTCTGCTCCTCTTTGGCCTCT , CM000675.1:g.28592970_28592971insTCTGCTCCTCTTTGGCCTCT GRCh37
NC_000013.9:g.27490970_27490971insTCTGCTCCTCTTTGGCCTCT NCBI36
NG_007066.1:g.86735_86736insAGAGGCCAAAGAGGAGCAGA , LRG_457:g.86735_86736insAGAGGCCAAAGAGGAGCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA MANE Select ENSP00000241453.7:n.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA
ENST00000241453.11:c.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA ENSP00000241453.7:n.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA
ENST00000380987.2:c.*331-245_*331-244insAGAGGCCAAAGAGGAGCAGA ENSP00000370374.2:n.*331-245_*331-244insAGAGGCCAAAGAGGAGCAGA
NM_004119.2:c.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA , LRG_457t1:c.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA NP_004110.2:n.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA
NR_130706.1:n.2633-245_2633-244insAGAGGCCAAAGAGGAGCAGA
XM_011535015.1:c.2362-245_2362-244insAGAGGCCAAAGAGGAGCAGA XP_011533317.1:n.2362-245_2362-244insAGAGGCCAAAGAGGAGCAGA
XM_011535016.1:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_011533318.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_011535017.1:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_011533319.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_011535018.1:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_011533320.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_011535015.2:c.2362-245_2362-244insAGAGGCCAAAGAGGAGCAGA XP_011533317.1:n.2362-245_2362-244insAGAGGCCAAAGAGGAGCAGA
XM_011535017.2:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_011533319.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_011535018.2:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_011533320.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_017020486.1:c.2203-245_2203-244insAGAGGCCAAAGAGGAGCAGA XP_016875975.1:n.2203-245_2203-244insAGAGGCCAAAGAGGAGCAGA
XM_017020487.1:c.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA XP_016875976.1:n.1894-245_1894-244insAGAGGCCAAAGAGGAGCAGA
XM_017020488.1:c.1540-245_1540-244insAGAGGCCAAAGAGGAGCAGA XP_016875977.1:n.1540-245_1540-244insAGAGGCCAAAGAGGAGCAGA
XM_017020489.1:c.1522-245_1522-244insAGAGGCCAAAGAGGAGCAGA XP_016875978.1:n.1522-245_1522-244insAGAGGCCAAAGAGGAGCAGA
NM_004119.3:c.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA MANE Select NP_004110.2:n.2419-245_2419-244insAGAGGCCAAAGAGGAGCAGA
NR_130706.2:n.2617-245_2617-244insAGAGGCCAAAGAGGAGCAGA