Canonical Allele Identifier: CA280208

Gene: FLT3

Linked Data

• ClinVar Variation Id: 16273
• ClinVar RCV Id: RCV000017662
• dbSNP Id: rs121913488
• COSMIC: COSM785
• MyVariant Identifiers: chr13:g.28592642C>G (hg19) ; chr13:g.28018505C>G (hg38)
• CIViC: CA280208
• PubMed: PMID:11290608 ; PMID:11442493 ; PMID:14604974 ; PMID:15256420 ; PMID:16857985 ; PMID:17047150 ; PMID:20733134 ; PMID:22368270 ; PMID:22504184 ; PMID:23261068 ; PMID:23321257 ; PMID:23430109 ; PMID:23714533 ; PMID:23783394 ; PMID:24046014 ; PMID:25157968

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