Canonical Allele Identifier: CA16602447

Gene: FLT3

Linked Data

• ClinVar Variation Id: 375970
• ClinVar RCV Id: RCV000432941
• dbSNP Id: rs1057519726
• COSMIC: COSM19649
• MyVariant Identifiers: chr13:g.28592639T>G (hg19) ; chr13:g.28018502T>G (hg38)
• PubMed: PMID:15863200 ; PMID:22368270 ; PMID:22504186 ; PMID:23261068 ; PMID:23321257 ; PMID:23714533 ; PMID:23783394

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018502T>G , CM000675.2:g.28018502T>G	GRCh38
NC_000013.10:g.28592639T>G , CM000675.1:g.28592639T>G	GRCh37
NC_000013.9:g.27490639T>G	NCBI36
NG_007066.1:g.87067A>C , LRG_457:g.87067A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2506A>C MANE Select	ENSP00000241453.7:p.Ile836Leu
ENST00000241453.11:c.2506A>C	ENSP00000241453.7:p.Ile836Leu
ENST00000380987.2:c.*418A>C	ENSP00000370374.2:n.*418A>C
NM_004119.2:c.2506A>C , LRG_457t1:c.2506A>C	NP_004110.2:p.Ile836Leu
NR_130706.1:n.2720A>C
XM_011535015.1:c.2449A>C	XP_011533317.1:p.Ile817Leu
XM_011535016.1:c.1981A>C	XP_011533318.1:p.Ile661Leu
XM_011535017.1:c.1981A>C	XP_011533319.1:p.Ile661Leu
XM_011535018.1:c.1981A>C	XP_011533320.1:p.Ile661Leu
XM_011535015.2:c.2449A>C	XP_011533317.1:p.Ile817Leu
XM_011535017.2:c.1981A>C	XP_011533319.1:p.Ile661Leu
XM_011535018.2:c.1981A>C	XP_011533320.1:p.Ile661Leu
XM_017020486.1:c.2290A>C	XP_016875975.1:p.Ile764Leu
XM_017020487.1:c.1981A>C	XP_016875976.1:p.Ile661Leu
XM_017020488.1:c.1627A>C	XP_016875977.1:p.Ile543Leu
XM_017020489.1:c.1609A>C	XP_016875978.1:p.Ile537Leu
NM_004119.3:c.2506A>C MANE Select	NP_004110.2:p.Ile836Leu
NR_130706.2:n.2704A>C