Canonical Allele Identifier: CA126347
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16276
ClinVar RCV Id: RCV000017665 RCV000017666
dbSNP Id: rs121913488
COSMIC: COSM783
MyVariant Identifiers: chr13:g.28592642C>A (hg19) chr13:g.28018505C>A (hg38)
CIViC: CA126347
PubMed: PMID:11290608 PMID:11442493 PMID:14670924 PMID:15256420 PMID:16857985 PMID:17889720 PMID:19657110 PMID:20733134 PMID:22368270 PMID:22504183 PMID:22504184 PMID:23261068 PMID:23321257 PMID:23430109 PMID:23714533 PMID:23783394 PMID:25157968
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018505C>A , CM000675.2:g.28018505C>A GRCh38
NC_000013.10:g.28592642C>A , CM000675.1:g.28592642C>A GRCh37
NC_000013.9:g.27490642C>A NCBI36
NG_007066.1:g.87064G>T , LRG_457:g.87064G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2503G>T MANE Select ENSP00000241453.7:p.Asp835Tyr
ENST00000241453.11:c.2503G>T ENSP00000241453.7:p.Asp835Tyr
ENST00000380987.2:c.*415G>T ENSP00000370374.2:n.*415G>T
NM_004119.2:c.2503G>T , LRG_457t1:c.2503G>T NP_004110.2:p.Asp835Tyr
NR_130706.1:n.2717G>T
XM_011535015.1:c.2446G>T XP_011533317.1:p.Asp816Tyr
XM_011535016.1:c.1978G>T XP_011533318.1:p.Asp660Tyr
XM_011535017.1:c.1978G>T XP_011533319.1:p.Asp660Tyr
XM_011535018.1:c.1978G>T XP_011533320.1:p.Asp660Tyr
XM_011535015.2:c.2446G>T XP_011533317.1:p.Asp816Tyr
XM_011535017.2:c.1978G>T XP_011533319.1:p.Asp660Tyr
XM_011535018.2:c.1978G>T XP_011533320.1:p.Asp660Tyr
XM_017020486.1:c.2287G>T XP_016875975.1:p.Asp763Tyr
XM_017020487.1:c.1978G>T XP_016875976.1:p.Asp660Tyr
XM_017020488.1:c.1624G>T XP_016875977.1:p.Asp542Tyr
XM_017020489.1:c.1606G>T XP_016875978.1:p.Asp536Tyr
NM_004119.3:c.2503G>T MANE Select NP_004110.2:p.Asp835Tyr
NR_130706.2:n.2701G>T
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