Canonical Allele Identifier: CA16602772
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 376326
ClinVar RCV Id: RCV000424567
dbSNP Id: rs121913490

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018500_28018502del , CM000675.2:g.28018500_28018502del GRCh38
NC_000013.10:g.28592637_28592639del , CM000675.1:g.28592637_28592639del GRCh37
NC_000013.9:g.27490637_27490639del NCBI36
NG_007066.1:g.87069_87071del , LRG_457:g.87069_87071del

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2508_2510del MANE Select ENSP00000241453.7:p.Ile836del
ENST00000241453.11:c.2508_2510del ENSP00000241453.7:p.Ile836del
ENST00000380987.2:c.*420_*422del ENSP00000370374.2:n.*420_*422del
NM_004119.2:c.2508_2510del , LRG_457t1:c.2508_2510del NP_004110.2:p.Ile836del
NR_130706.1:n.2722_2724del
XM_011535015.1:c.2451_2453del XP_011533317.1:p.Ile817del
XM_011535016.1:c.1983_1985del XP_011533318.1:p.Ile661del
XM_011535017.1:c.1983_1985del XP_011533319.1:p.Ile661del
XM_011535018.1:c.1983_1985del XP_011533320.1:p.Ile661del
XM_011535015.2:c.2451_2453del XP_011533317.1:p.Ile817del
XM_011535017.2:c.1983_1985del XP_011533319.1:p.Ile661del
XM_011535018.2:c.1983_1985del XP_011533320.1:p.Ile661del
XM_017020486.1:c.2292_2294del XP_016875975.1:p.Ile764del
XM_017020487.1:c.1983_1985del XP_016875976.1:p.Ile661del
XM_017020488.1:c.1629_1631del XP_016875977.1:p.Ile543del
XM_017020489.1:c.1611_1613del XP_016875978.1:p.Ile537del
NM_004119.3:c.2508_2510del MANE Select NP_004110.2:p.Ile836del
NR_130706.2:n.2706_2708del