Canonical Allele Identifier: CA2575379128
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018380_28018385del , CM000675.2:g.28018380_28018385del GRCh38
NC_000013.10:g.28592517_28592522del , CM000675.1:g.28592517_28592522del GRCh37
NC_000013.9:g.27490517_27490522del NCBI36
NG_007066.1:g.87184_87189del , LRG_457:g.87184_87189del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2541+82_2541+87del MANE Select ENSP00000241453.7:n.2541+82_2541+87del
ENST00000241453.11:c.2541+82_2541+87del ENSP00000241453.7:n.2541+82_2541+87del
ENST00000380987.2:c.*453+82_*453+87del ENSP00000370374.2:n.*453+82_*453+87del
NM_004119.2:c.2541+82_2541+87del , LRG_457t1:c.2541+82_2541+87del NP_004110.2:n.2541+82_2541+87del
NR_130706.1:n.2755+82_2755+87del
XM_011535015.1:c.2484+82_2484+87del XP_011533317.1:n.2484+82_2484+87del
XM_011535016.1:c.2016+82_2016+87del XP_011533318.1:n.2016+82_2016+87del
XM_011535017.1:c.2016+82_2016+87del XP_011533319.1:n.2016+82_2016+87del
XM_011535018.1:c.2016+82_2016+87del XP_011533320.1:n.2016+82_2016+87del
XM_011535015.2:c.2484+82_2484+87del XP_011533317.1:n.2484+82_2484+87del
XM_011535017.2:c.2016+82_2016+87del XP_011533319.1:n.2016+82_2016+87del
XM_011535018.2:c.2016+82_2016+87del XP_011533320.1:n.2016+82_2016+87del
XM_017020486.1:c.2325+82_2325+87del XP_016875975.1:n.2325+82_2325+87del
XM_017020487.1:c.2016+82_2016+87del XP_016875976.1:n.2016+82_2016+87del
XM_017020488.1:c.1662+82_1662+87del XP_016875977.1:n.1662+82_1662+87del
XM_017020489.1:c.1644+82_1644+87del XP_016875978.1:n.1644+82_1644+87del
NM_004119.3:c.2541+82_2541+87del MANE Select NP_004110.2:n.2541+82_2541+87del
NR_130706.2:n.2739+82_2739+87del