Canonical Allele Identifier: CA16602446

Gene: FLT3

Linked Data

• ClinVar Variation Id: 375969
• ClinVar RCV Id: RCV000422249
• dbSNP Id: rs121913232
• COSMIC: COSM19686
• MyVariant Identifiers: chr13:g.28592637G>C (hg19) ; chr13:g.28018500G>C (hg38)
• PubMed: PMID:19840437 ; PMID:22368270 ; PMID:22504186 ; PMID:23261068 ; PMID:23321257 ; PMID:23714533 ; PMID:23783394 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018500G>C , CM000675.2:g.28018500G>C	GRCh38
NC_000013.10:g.28592637G>C , CM000675.1:g.28592637G>C	GRCh37
NC_000013.9:g.27490637G>C	NCBI36
NG_007066.1:g.87069C>G , LRG_457:g.87069C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2508C>G MANE Select	ENSP00000241453.7:p.Ile836Met
ENST00000241453.11:c.2508C>G	ENSP00000241453.7:p.Ile836Met
ENST00000380987.2:c.*420C>G	ENSP00000370374.2:n.*420C>G
NM_004119.2:c.2508C>G , LRG_457t1:c.2508C>G	NP_004110.2:p.Ile836Met
NR_130706.1:n.2722C>G
XM_011535015.1:c.2451C>G	XP_011533317.1:p.Ile817Met
XM_011535016.1:c.1983C>G	XP_011533318.1:p.Ile661Met
XM_011535017.1:c.1983C>G	XP_011533319.1:p.Ile661Met
XM_011535018.1:c.1983C>G	XP_011533320.1:p.Ile661Met
XM_011535015.2:c.2451C>G	XP_011533317.1:p.Ile817Met
XM_011535017.2:c.1983C>G	XP_011533319.1:p.Ile661Met
XM_011535018.2:c.1983C>G	XP_011533320.1:p.Ile661Met
XM_017020486.1:c.2292C>G	XP_016875975.1:p.Ile764Met
XM_017020487.1:c.1983C>G	XP_016875976.1:p.Ile661Met
XM_017020488.1:c.1629C>G	XP_016875977.1:p.Ile543Met
XM_017020489.1:c.1611C>G	XP_016875978.1:p.Ile537Met
NM_004119.3:c.2508C>G MANE Select	NP_004110.2:p.Ile836Met
NR_130706.2:n.2706C>G