Canonical Allele Identifier: CA126344
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16272
ClinVar RCV Id: RCV000017660 RCV000017661
dbSNP Id: rs121909646
COSMIC: COSM784
MyVariant Identifiers: chr13:g.28592641T>A (hg19) chr13:g.28018504T>A (hg38)
CIViC: CA126344
PubMed: PMID:11290608 PMID:14604974 PMID:14670924 PMID:15256420 PMID:16857985 PMID:17606455 PMID:19657110 PMID:20733134 PMID:22368270 PMID:22504183 PMID:22504184 PMID:23261068 PMID:23321257 PMID:23430109 PMID:23714533 PMID:23783394 PMID:24046014 PMID:25157968
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018504T>A , CM000675.2:g.28018504T>A GRCh38
NC_000013.10:g.28592641T>A , CM000675.1:g.28592641T>A GRCh37
NC_000013.9:g.27490641T>A NCBI36
NG_007066.1:g.87065A>T , LRG_457:g.87065A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2504A>T MANE Select ENSP00000241453.7:p.Asp835Val
ENST00000241453.11:c.2504A>T ENSP00000241453.7:p.Asp835Val
ENST00000380987.2:c.*416A>T ENSP00000370374.2:n.*416A>T
NM_004119.2:c.2504A>T , LRG_457t1:c.2504A>T NP_004110.2:p.Asp835Val
NR_130706.1:n.2718A>T
XM_011535015.1:c.2447A>T XP_011533317.1:p.Asp816Val
XM_011535016.1:c.1979A>T XP_011533318.1:p.Asp660Val
XM_011535017.1:c.1979A>T XP_011533319.1:p.Asp660Val
XM_011535018.1:c.1979A>T XP_011533320.1:p.Asp660Val
XM_011535015.2:c.2447A>T XP_011533317.1:p.Asp816Val
XM_011535017.2:c.1979A>T XP_011533319.1:p.Asp660Val
XM_011535018.2:c.1979A>T XP_011533320.1:p.Asp660Val
XM_017020486.1:c.2288A>T XP_016875975.1:p.Asp763Val
XM_017020487.1:c.1979A>T XP_016875976.1:p.Asp660Val
XM_017020488.1:c.1625A>T XP_016875977.1:p.Asp542Val
XM_017020489.1:c.1607A>T XP_016875978.1:p.Asp536Val
NM_004119.3:c.2504A>T MANE Select NP_004110.2:p.Asp835Val
NR_130706.2:n.2702A>T
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