Canonical Allele Identifier: CA2573131833

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034115_28034116insTGCAAACTCTAAATTTTCTCTTGGAAACTCCCATTT , CM000675.2:g.28034115_28034116insTGCAAACTCTAAATTTTCTCTTGGAAACTCCCATTT	GRCh38
NC_000013.10:g.28608252_28608253insTGCAAACTCTAAATTTTCTCTTGGAAACTCCCATTT , CM000675.1:g.28608252_28608253insTGCAAACTCTAAATTTTCTCTTGGAAACTCCCATTT	GRCh37
NC_000013.9:g.27506252_27506253insTGCAAACTCTAAATTTTCTCTTGGAAACTCCCATTT	NCBI36
NG_007066.1:g.71487_71488insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457:g.71487_71488insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select	ENSP00000241453.7:p.Phe612_Gly613insAlaLysTrpGluPheProArgGluA...
ENST00000241453.11:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	ENSP00000241453.7:p.Phe612_Gly613insAlaLysTrpGluPheProArgGluA...
ENST00000380987.2:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	ENSP00000370374.2:p.Phe612_Gly613insAlaLysTrpGluPheProArgGluA...
NM_004119.2:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG , LRG_457t1:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	NP_004110.2:p.Phe612_Gly613insAlaLysTrpGluPheProArgGluAsnLeuG...
NR_130706.1:n.1919_1919+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG
XM_011535015.1:c.1780_1780+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533317.1:p.Phe593_Gly594insAlaLysTrpGluPheProArgGluAsnL...
XM_011535016.1:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533318.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_011535017.1:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533319.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_011535018.1:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533320.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_011535015.2:c.1780_1780+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533317.1:p.Phe593_Gly594insAlaLysTrpGluPheProArgGluAsnL...
XM_011535017.2:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533319.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_011535018.2:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_011533320.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_017020486.1:c.1621_1621+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_016875975.1:p.Phe540_Gly541insAlaLysTrpGluPheProArgGluAsnL...
XM_017020487.1:c.1312_1312+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_016875976.1:p.Phe437_Gly438insAlaLysTrpGluPheProArgGluAsnL...
XM_017020488.1:c.958_958+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_016875977.1:p.Phe319_Gly320insAlaLysTrpGluPheProArgGluAsnL...
XM_017020489.1:c.940_940+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG	XP_016875978.1:p.Phe313_Gly314insAlaLysTrpGluPheProArgGluAsnL...
NM_004119.3:c.1837_1837+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG MANE Select	NP_004110.2:p.Phe612_Gly613insAlaLysTrpGluPheProArgGluAsnLeuG...
NR_130706.2:n.1903_1903+1insCAAAATGGGAGTTTCCAAGAGAAAATTTAGAGTTTG