Canonical Allele Identifier: CA645597696

Gene: FLT3

Linked Data

• COSMIC: COSM851

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018504_28018509del , CM000675.2:g.28018504_28018509del	GRCh38
NC_000013.10:g.28592641_28592646del , CM000675.1:g.28592641_28592646del	GRCh37
NC_000013.9:g.27490641_27490646del	NCBI36
NG_007066.1:g.87061_87066del , LRG_457:g.87061_87066del

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2500_2505del MANE Select	ENSP00000241453.7:p.Arg834_Asp835del
ENST00000241453.11:c.2500_2505del	ENSP00000241453.7:p.Arg834_Asp835del
ENST00000380987.2:c.*412_*417del	ENSP00000370374.2:n.*412_*417del
NM_004119.2:c.2500_2505del , LRG_457t1:c.2500_2505del	NP_004110.2:p.Arg834_Asp835del
NR_130706.1:n.2714_2719del
XM_011535015.1:c.2443_2448del	XP_011533317.1:p.Arg815_Asp816del
XM_011535016.1:c.1975_1980del	XP_011533318.1:p.Arg659_Asp660del
XM_011535017.1:c.1975_1980del	XP_011533319.1:p.Arg659_Asp660del
XM_011535018.1:c.1975_1980del	XP_011533320.1:p.Arg659_Asp660del
XM_011535015.2:c.2443_2448del	XP_011533317.1:p.Arg815_Asp816del
XM_011535017.2:c.1975_1980del	XP_011533319.1:p.Arg659_Asp660del
XM_011535018.2:c.1975_1980del	XP_011533320.1:p.Arg659_Asp660del
XM_017020486.1:c.2284_2289del	XP_016875975.1:p.Arg762_Asp763del
XM_017020487.1:c.1975_1980del	XP_016875976.1:p.Arg659_Asp660del
XM_017020488.1:c.1621_1626del	XP_016875977.1:p.Arg541_Asp542del
XM_017020489.1:c.1603_1608del	XP_016875978.1:p.Arg535_Asp536del
NM_004119.3:c.2500_2505del MANE Select	NP_004110.2:p.Arg834_Asp835del
NR_130706.2:n.2698_2703del