Canonical Allele Identifier: CA3202185969
Community Standard Title: NM_004119.3(FLT3):c.2490T= (p.Phe830=)
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018518A= , CM000675.2:g.28018518A= GRCh38
NC_000013.10:g.28592655A= , CM000675.1:g.28592655A= GRCh37
NC_000013.9:g.27490655A= NCBI36
NG_007066.1:g.87051T= , LRG_457:g.87051T=

Transcript Alleles

HGVS Amino-acid Change
NM_004119.3:c.2490T= MANE Select NP_004110.2:p.Phe830=
ENST00000241453.12:c.2490T= MANE Select ENSP00000241453.7:p.Phe830=
NM_004119.2:c.2490T= , LRG_457t1:c.2490T= NP_004110.2:p.Phe830=
NR_130706.1:n.2704T=
NR_130706.2:n.2688T=
ENST00000241453.11:c.2490T= ENSP00000241453.7:p.Phe830=
ENST00000380987.2:c.*402T= ENSP00000370374.2:n.*402T=
XM_011535015.1:c.2433T= XP_011533317.1:p.Phe811=
XM_011535015.2:c.2433T= XP_011533317.1:p.Phe811=
XM_011535016.1:c.1965T= XP_011533318.1:p.Phe655=
XM_011535017.1:c.1965T= XP_011533319.1:p.Phe655=
XM_011535017.2:c.1965T= XP_011533319.1:p.Phe655=
XM_011535018.1:c.1965T= XP_011533320.1:p.Phe655=
XM_011535018.2:c.1965T= XP_011533320.1:p.Phe655=
XM_017020486.1:c.2274T= XP_016875975.1:p.Phe758=
XM_017020487.1:c.1965T= XP_016875976.1:p.Phe655=
XM_017020488.1:c.1611T= XP_016875977.1:p.Phe537=
XM_017020489.1:c.1593T= XP_016875978.1:p.Phe531=