Canonical Allele Identifier: CA913184837
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018476_28018477insTCG , CM000675.2:g.28018476_28018477insTCG GRCh38
NC_000013.10:g.28592613_28592614insTCG , CM000675.1:g.28592613_28592614insTCG GRCh37
NC_000013.9:g.27490613_27490614insTCG NCBI36
NG_007066.1:g.87093_87094insGAC , LRG_457:g.87093_87094insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2532_2533insGAC MANE Select ENSP00000241453.7:p.Val844_Arg845insAsp
ENST00000241453.11:c.2532_2533insGAC ENSP00000241453.7:p.Val844_Arg845insAsp
ENST00000380987.2:c.*444_*445insGAC ENSP00000370374.2:n.*444_*445insGAC
NM_004119.2:c.2532_2533insGAC , LRG_457t1:c.2532_2533insGAC NP_004110.2:p.Val844_Arg845insAsp
NR_130706.1:n.2746_2747insGAC
XM_011535015.1:c.2475_2476insGAC XP_011533317.1:p.Val825_Arg826insAsp
XM_011535016.1:c.2007_2008insGAC XP_011533318.1:p.Val669_Arg670insAsp
XM_011535017.1:c.2007_2008insGAC XP_011533319.1:p.Val669_Arg670insAsp
XM_011535018.1:c.2007_2008insGAC XP_011533320.1:p.Val669_Arg670insAsp
XM_011535015.2:c.2475_2476insGAC XP_011533317.1:p.Val825_Arg826insAsp
XM_011535017.2:c.2007_2008insGAC XP_011533319.1:p.Val669_Arg670insAsp
XM_011535018.2:c.2007_2008insGAC XP_011533320.1:p.Val669_Arg670insAsp
XM_017020486.1:c.2316_2317insGAC XP_016875975.1:p.Val772_Arg773insAsp
XM_017020487.1:c.2007_2008insGAC XP_016875976.1:p.Val669_Arg670insAsp
XM_017020488.1:c.1653_1654insGAC XP_016875977.1:p.Val551_Arg552insAsp
XM_017020489.1:c.1635_1636insGAC XP_016875978.1:p.Val545_Arg546insAsp
NM_004119.3:c.2532_2533insGAC MANE Select NP_004110.2:p.Val844_Arg845insAsp
NR_130706.2:n.2730_2731insGAC