Canonical Allele Identifier: CA2080781027
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018089T= , CM000675.2:g.28018089T= GRCh38
NC_000013.10:g.28592226T= , CM000675.1:g.28592226T= GRCh37
NC_000013.9:g.27490226T= NCBI36
NG_007066.1:g.87480A= , LRG_457:g.87480A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2541+378A= MANE Select ENSP00000241453.7:n.2541+378A=
ENST00000241453.11:c.2541+378A= ENSP00000241453.7:n.2541+378A=
ENST00000380987.2:c.*453+378A= ENSP00000370374.2:n.*453+378A=
NM_004119.2:c.2541+378A= , LRG_457t1:c.2541+378A= NP_004110.2:n.2541+378A=
NR_130706.1:n.2755+378A=
XM_011535015.1:c.2484+378A= XP_011533317.1:n.2484+378A=
XM_011535016.1:c.2016+378A= XP_011533318.1:n.2016+378A=
XM_011535017.1:c.2016+378A= XP_011533319.1:n.2016+378A=
XM_011535018.1:c.2016+378A= XP_011533320.1:n.2016+378A=
XM_011535015.2:c.2484+378A= XP_011533317.1:n.2484+378A=
XM_011535017.2:c.2016+378A= XP_011533319.1:n.2016+378A=
XM_011535018.2:c.2016+378A= XP_011533320.1:n.2016+378A=
XM_017020486.1:c.2325+378A= XP_016875975.1:n.2325+378A=
XM_017020487.1:c.2016+378A= XP_016875976.1:n.2016+378A=
XM_017020488.1:c.1662+378A= XP_016875977.1:n.1662+378A=
XM_017020489.1:c.1644+378A= XP_016875978.1:n.1644+378A=
NM_004119.3:c.2541+378A= MANE Select NP_004110.2:n.2541+378A=
NR_130706.2:n.2739+378A=