Canonical Allele Identifier: CA915940311

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018492_28018494del , CM000675.2:g.28018492_28018494del	GRCh38
NC_000013.10:g.28592629_28592631del , CM000675.1:g.28592629_28592631del	GRCh37
NC_000013.9:g.27490629_27490631del	NCBI36
NG_007066.1:g.87076_87078del , LRG_457:g.87076_87078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2515_2517del MANE Select	ENSP00000241453.7:p.Asp839del
ENST00000241453.11:c.2515_2517del	ENSP00000241453.7:p.Asp839del
ENST00000380987.2:c.*427_*429del	ENSP00000370374.2:n.*427_*429del
NM_004119.2:c.2515_2517del , LRG_457t1:c.2515_2517del	NP_004110.2:p.Asp839del
NR_130706.1:n.2729_2731del
XM_011535015.1:c.2458_2460del	XP_011533317.1:p.Asp820del
XM_011535016.1:c.1990_1992del	XP_011533318.1:p.Asp664del
XM_011535017.1:c.1990_1992del	XP_011533319.1:p.Asp664del
XM_011535018.1:c.1990_1992del	XP_011533320.1:p.Asp664del
XM_011535015.2:c.2458_2460del	XP_011533317.1:p.Asp820del
XM_011535017.2:c.1990_1992del	XP_011533319.1:p.Asp664del
XM_011535018.2:c.1990_1992del	XP_011533320.1:p.Asp664del
XM_017020486.1:c.2299_2301del	XP_016875975.1:p.Asp767del
XM_017020487.1:c.1990_1992del	XP_016875976.1:p.Asp664del
XM_017020488.1:c.1636_1638del	XP_016875977.1:p.Asp546del
XM_017020489.1:c.1618_1620del	XP_016875978.1:p.Asp540del
NM_004119.3:c.2515_2517del MANE Select	NP_004110.2:p.Asp839del
NR_130706.2:n.2713_2715del