Canonical Allele Identifier: CA891842181

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034174_28034175insAGGGGACGGTACCAAACTCTAAATTTTCTCTTGGAAAC , CM000675.2:g.28034174_28034175insAGGGGACGGTACCAAACTCTAAATTTTCTCTTGGAAAC	GRCh38
NC_000013.10:g.28608311_28608312insAGGGGACGGTACCAAACTCTAAATTTTCTCTTGGAAAC , CM000675.1:g.28608311_28608312insAGGGGACGGTACCAAACTCTAAATTTTCTCTTGGAAAC	GRCh37
NC_000013.9:g.27506311_27506312insAGGGGACGGTACCAAACTCTAAATTTTCTCTTGGAAAC	NCBI36
NG_007066.1:g.71394_71395insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT , LRG_457:g.71394_71395insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT MANE Select	ENSP00000241453.7:p.Thr582SerfsTer7
ENST00000241453.11:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	ENSP00000241453.7:p.Thr582SerfsTer7
ENST00000380987.2:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	ENSP00000370374.2:p.Thr582SerfsTer7
NM_004119.2:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT , LRG_457t1:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	NP_004110.2:p.Thr582SerfsTer7
NR_130706.1:n.1826_1827insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT
XM_011535015.1:c.1687_1688insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533317.1:p.Thr563SerfsTer7
XM_011535016.1:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533318.1:p.Thr407SerfsTer7
XM_011535017.1:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533319.1:p.Thr407SerfsTer7
XM_011535018.1:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533320.1:p.Thr407SerfsTer7
XM_011535015.2:c.1687_1688insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533317.1:p.Thr563SerfsTer7
XM_011535017.2:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533319.1:p.Thr407SerfsTer7
XM_011535018.2:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_011533320.1:p.Thr407SerfsTer7
XM_017020486.1:c.1528_1529insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_016875975.1:p.Thr510SerfsTer7
XM_017020487.1:c.1219_1220insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_016875976.1:p.Thr407SerfsTer7
XM_017020488.1:c.865_866insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_016875977.1:p.Thr289SerfsTer7
XM_017020489.1:c.847_848insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT	XP_016875978.1:p.Thr283SerfsTer7
NM_004119.3:c.1744_1745insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT MANE Select	NP_004110.2:p.Thr582SerfsTer7
NR_130706.2:n.1810_1811insGTTTCCAAGAGAAAATTTAGAGTTTGGTACCGTCCCCT