Canonical Allele Identifier: CA16602449

Gene: FLT3

Linked Data

• ClinVar Variation Id: 375972
• ClinVar RCV Id: RCV000424615
• dbSNP Id: rs121913487
• MyVariant Identifiers: chr13:g.28592640A>T (hg19) ; chr13:g.28018503A>T (hg38)
• CIViC: CA16602449
• PubMed: PMID:11290608 ; PMID:15256420 ; PMID:15374878 ; PMID:16857985 ; PMID:19657110 ; PMID:20733134 ; PMID:22368270 ; PMID:22504183 ; PMID:22504184 ; PMID:23261068 ; PMID:23321257 ; PMID:23430109 ; PMID:23714533 ; PMID:23783394 ; PMID:25157968

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018503A>T , CM000675.2:g.28018503A>T	GRCh38
NC_000013.10:g.28592640A>T , CM000675.1:g.28592640A>T	GRCh37
NC_000013.9:g.27490640A>T	NCBI36
NG_007066.1:g.87066T>A , LRG_457:g.87066T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2505T>A MANE Select	ENSP00000241453.7:p.Asp835Glu
ENST00000241453.11:c.2505T>A	ENSP00000241453.7:p.Asp835Glu
ENST00000380987.2:c.*417T>A	ENSP00000370374.2:n.*417T>A
NM_004119.2:c.2505T>A , LRG_457t1:c.2505T>A	NP_004110.2:p.Asp835Glu
NR_130706.1:n.2719T>A
XM_011535015.1:c.2448T>A	XP_011533317.1:p.Asp816Glu
XM_011535016.1:c.1980T>A	XP_011533318.1:p.Asp660Glu
XM_011535017.1:c.1980T>A	XP_011533319.1:p.Asp660Glu
XM_011535018.1:c.1980T>A	XP_011533320.1:p.Asp660Glu
XM_011535015.2:c.2448T>A	XP_011533317.1:p.Asp816Glu
XM_011535017.2:c.1980T>A	XP_011533319.1:p.Asp660Glu
XM_011535018.2:c.1980T>A	XP_011533320.1:p.Asp660Glu
XM_017020486.1:c.2289T>A	XP_016875975.1:p.Asp763Glu
XM_017020487.1:c.1980T>A	XP_016875976.1:p.Asp660Glu
XM_017020488.1:c.1626T>A	XP_016875977.1:p.Asp542Glu
XM_017020489.1:c.1608T>A	XP_016875978.1:p.Asp536Glu
NM_004119.3:c.2505T>A MANE Select	NP_004110.2:p.Asp835Glu
NR_130706.2:n.2703T>A