Canonical Allele Identifier: CA645598040

Gene: FLT3

Linked Data

• COSMIC: COSM5985581

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034171_28034172insAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCTAC , CM000675.2:g.28034171_28034172insAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCTAC	GRCh38
NC_000013.10:g.28608308_28608309insAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCTAC , CM000675.1:g.28608308_28608309insAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCTAC	GRCh37
NC_000013.9:g.27506308_27506309insAACTCCCATTTGAGATCATATTCATATTCTCTGAAATCAACGTAGAAGTACTCATTATCTGAGGAGCTAC	NCBI36
NG_007066.1:g.71398_71399insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG , LRG_457:g.71398_71399insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG MANE Select	ENSP00000241453.7:p.Asp586SerfsTer25
ENST00000241453.11:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	ENSP00000241453.7:p.Asp586SerfsTer25
ENST00000380987.2:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	ENSP00000370374.2:p.Asp586SerfsTer25
NM_004119.2:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG , LRG_457t1:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	NP_004110.2:p.Asp586SerfsTer25
NR_130706.1:n.1830_1831insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG
XM_011535015.1:c.1691_1692insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533317.1:p.Asp567SerfsTer25
XM_011535016.1:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533318.1:p.Asp411SerfsTer25
XM_011535017.1:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533319.1:p.Asp411SerfsTer25
XM_011535018.1:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533320.1:p.Asp411SerfsTer25
XM_011535015.2:c.1691_1692insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533317.1:p.Asp567SerfsTer25
XM_011535017.2:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533319.1:p.Asp411SerfsTer25
XM_011535018.2:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_011533320.1:p.Asp411SerfsTer25
XM_017020486.1:c.1532_1533insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_016875975.1:p.Asp514SerfsTer25
XM_017020487.1:c.1223_1224insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_016875976.1:p.Asp411SerfsTer25
XM_017020488.1:c.869_870insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_016875977.1:p.Asp293SerfsTer25
XM_017020489.1:c.851_852insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG	XP_016875978.1:p.Asp287SerfsTer25
NM_004119.3:c.1748_1749insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG MANE Select	NP_004110.2:p.Asp586SerfsTer25
NR_130706.2:n.1814_1815insTAGCTCCTCAGATAATGAGTACTTCTACGTTGATTTCAGAGAATATGAATATGATCTCAAATGGGAGTTG