Canonical Allele Identifier: CA280214
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16277
ClinVar RCV Id: RCV000017667
dbSNP Id: rs121913486
COSMIC: COSM796 COSM854
MyVariant Identifiers: chr13:g.28592640_28592642del (hg19) chr13:g.28018503_28018505del (hg38)
PubMed: PMID:11442493 PMID:25157968
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018503_28018505del , CM000675.2:g.28018503_28018505del GRCh38
NC_000013.10:g.28592640_28592642del , CM000675.1:g.28592640_28592642del GRCh37
NC_000013.9:g.27490640_27490642del NCBI36
NG_007066.1:g.87064_87066del , LRG_457:g.87064_87066del

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2503_2505del MANE Select ENSP00000241453.7:p.Asp835del
ENST00000241453.11:c.2503_2505del ENSP00000241453.7:p.Asp835del
ENST00000380987.2:c.*415_*417del ENSP00000370374.2:n.*415_*417del
NM_004119.2:c.2503_2505del , LRG_457t1:c.2503_2505del NP_004110.2:p.Asp835del
NR_130706.1:n.2717_2719del
XM_011535015.1:c.2446_2448del XP_011533317.1:p.Asp816del
XM_011535016.1:c.1978_1980del XP_011533318.1:p.Asp660del
XM_011535017.1:c.1978_1980del XP_011533319.1:p.Asp660del
XM_011535018.1:c.1978_1980del XP_011533320.1:p.Asp660del
XM_011535015.2:c.2446_2448del XP_011533317.1:p.Asp816del
XM_011535017.2:c.1978_1980del XP_011533319.1:p.Asp660del
XM_011535018.2:c.1978_1980del XP_011533320.1:p.Asp660del
XM_017020486.1:c.2287_2289del XP_016875975.1:p.Asp763del
XM_017020487.1:c.1978_1980del XP_016875976.1:p.Asp660del
XM_017020488.1:c.1624_1626del XP_016875977.1:p.Asp542del
XM_017020489.1:c.1606_1608del XP_016875978.1:p.Asp536del
NM_004119.3:c.2503_2505del MANE Select NP_004110.2:p.Asp835del
NR_130706.2:n.2701_2703del
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