Canonical Allele Identifier: CA2742038405
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034087_28034088insAGGGTGCGCCCGCGCAGCGCCACCAAACT , CM000675.2:g.28034087_28034088insAGGGTGCGCCCGCGCAGCGCCACCAAACT GRCh38
NC_000013.10:g.28608224_28608225insAGGGTGCGCCCGCGCAGCGCCACCAAACT , CM000675.1:g.28608224_28608225insAGGGTGCGCCCGCGCAGCGCCACCAAACT GRCh37
NC_000013.9:g.27506224_27506225insAGGGTGCGCCCGCGCAGCGCCACCAAACT NCBI36
NG_007066.1:g.71489_71490insGGCGCTGCGCGGGCGCACCCTAGTTTGGT , LRG_457:g.71489_71490insGGCGCTGCGCGGGCGCACCCTAGTTTGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
ENST00000241453.11:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
ENST00000380987.2:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
NM_004119.2:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT , LRG_457t1:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
NR_130706.1:n.1919+2_1919+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535015.1:c.1780+2_1780+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535016.1:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535017.1:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535018.1:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535015.2:c.1780+2_1780+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535017.2:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_011535018.2:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_017020486.1:c.1621+2_1621+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_017020487.1:c.1312+2_1312+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_017020488.1:c.958+2_958+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
XM_017020489.1:c.940+2_940+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
NM_004119.3:c.1837+2_1837+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT
NR_130706.2:n.1903+2_1903+3insGGCGCTGCGCGGGCGCACCCTAGTTTGGT