Canonical Allele Identifier: CA2622474734
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018567del , CM000675.2:g.28018567del GRCh38
NC_000013.10:g.28592704del , CM000675.1:g.28592704del GRCh37
NC_000013.9:g.27490704del NCBI36
NG_007066.1:g.87003del , LRG_457:g.87003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2442del MANE Select ENSP00000241453.7:p.Arg815GlyfsTer11
ENST00000241453.11:c.2442del ENSP00000241453.7:p.Arg815GlyfsTer11
ENST00000380987.2:c.*354del ENSP00000370374.2:n.*354del
NM_004119.2:c.2442del , LRG_457t1:c.2442del NP_004110.2:p.Arg815GlyfsTer11
NR_130706.1:n.2656del
XM_011535015.1:c.2385del XP_011533317.1:p.Arg796GlyfsTer11
XM_011535016.1:c.1917del XP_011533318.1:p.Arg640GlyfsTer11
XM_011535017.1:c.1917del XP_011533319.1:p.Arg640GlyfsTer11
XM_011535018.1:c.1917del XP_011533320.1:p.Arg640GlyfsTer11
XM_011535015.2:c.2385del XP_011533317.1:p.Arg796GlyfsTer11
XM_011535017.2:c.1917del XP_011533319.1:p.Arg640GlyfsTer11
XM_011535018.2:c.1917del XP_011533320.1:p.Arg640GlyfsTer11
XM_017020486.1:c.2226del XP_016875975.1:p.Arg743GlyfsTer11
XM_017020487.1:c.1917del XP_016875976.1:p.Arg640GlyfsTer11
XM_017020488.1:c.1563del XP_016875977.1:p.Arg522GlyfsTer11
XM_017020489.1:c.1545del XP_016875978.1:p.Arg516GlyfsTer11
NM_004119.3:c.2442del MANE Select NP_004110.2:p.Arg815GlyfsTer11
NR_130706.2:n.2640del