Canonical Allele Identifier: CA645597695

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623118
• COSMIC: COSM27651

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018502_28018504del , CM000675.2:g.28018502_28018504del	GRCh38
NC_000013.10:g.28592639_28592641del , CM000675.1:g.28592639_28592641del	GRCh37
NC_000013.9:g.27490639_27490641del	NCBI36
NG_007066.1:g.87065_87067del , LRG_457:g.87065_87067del

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2504_2506del MANE Select	ENSP00000241453.7:p.Asp835_Ile836delinsVa...
ENST00000241453.11:c.2504_2506del	ENSP00000241453.7:p.Asp835_Ile836delinsVa...
ENST00000380987.2:c.*416_*418del	ENSP00000370374.2:n.*416_*418del
NM_004119.2:c.2504_2506del , LRG_457t1:c.2504_2506del	NP_004110.2:p.Asp835_Ile836delinsVal
NR_130706.1:n.2718_2720del
XM_011535015.1:c.2447_2449del	XP_011533317.1:p.Asp816_Ile817delinsVal
XM_011535016.1:c.1979_1981del	XP_011533318.1:p.Asp660_Ile661delinsVal
XM_011535017.1:c.1979_1981del	XP_011533319.1:p.Asp660_Ile661delinsVal
XM_011535018.1:c.1979_1981del	XP_011533320.1:p.Asp660_Ile661delinsVal
XM_011535015.2:c.2447_2449del	XP_011533317.1:p.Asp816_Ile817delinsVal
XM_011535017.2:c.1979_1981del	XP_011533319.1:p.Asp660_Ile661delinsVal
XM_011535018.2:c.1979_1981del	XP_011533320.1:p.Asp660_Ile661delinsVal
XM_017020486.1:c.2288_2290del	XP_016875975.1:p.Asp763_Ile764delinsVal
XM_017020487.1:c.1979_1981del	XP_016875976.1:p.Asp660_Ile661delinsVal
XM_017020488.1:c.1625_1627del	XP_016875977.1:p.Asp542_Ile543delinsVal
XM_017020489.1:c.1607_1609del	XP_016875978.1:p.Asp536_Ile537delinsVal
NM_004119.3:c.2504_2506del MANE Select	NP_004110.2:p.Asp835_Ile836delinsVal
NR_130706.2:n.2702_2704del