Canonical Allele Identifier: CA280208
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16273
ClinVar RCV Id: RCV000017662
dbSNP Id: rs121913488
COSMIC: COSM785
CIViC: CA280208

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2503G>C MANE Select ENSP00000241453.7:p.Asp835His
ENST00000241453.11:c.2503G>C ENSP00000241453.7:p.Asp835His
ENST00000380987.2:c.*415G>C ENSP00000370374.2:n.*415G>C
NM_004119.2:c.2503G>C , LRG_457t1:c.2503G>C NP_004110.2:p.Asp835His
NR_130706.1:n.2717G>C
XM_011535015.1:c.2446G>C XP_011533317.1:p.Asp816His
XM_011535016.1:c.1978G>C XP_011533318.1:p.Asp660His
XM_011535017.1:c.1978G>C XP_011533319.1:p.Asp660His
XM_011535018.1:c.1978G>C XP_011533320.1:p.Asp660His
XM_011535015.2:c.2446G>C XP_011533317.1:p.Asp816His
XM_011535017.2:c.1978G>C XP_011533319.1:p.Asp660His
XM_011535018.2:c.1978G>C XP_011533320.1:p.Asp660His
XM_017020486.1:c.2287G>C XP_016875975.1:p.Asp763His
XM_017020487.1:c.1978G>C XP_016875976.1:p.Asp660His
XM_017020488.1:c.1624G>C XP_016875977.1:p.Asp542His
XM_017020489.1:c.1606G>C XP_016875978.1:p.Asp536His
NM_004119.3:c.2503G>C MANE Select NP_004110.2:p.Asp835His
NR_130706.2:n.2701G>C