Canonical Allele Identifier: CA126350

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034141_28034143del , CM000675.2:g.28034141_28034143del	GRCh38
NC_000013.10:g.28608278_28608280del , CM000675.1:g.28608278_28608280del	GRCh37
NC_000013.9:g.27506278_27506280del	NCBI36
NG_007066.1:g.71427_71429del , LRG_457:g.71427_71429del

Transcript Alleles

HGVS	Amino-acid Change
NM_004119.3:c.1777_1779del MANE Select	NP_004110.2:p.Asp593del
ENST00000241453.12:c.1777_1779del MANE Select	ENSP00000241453.7:p.Asp593del
NM_004119.2:c.1777_1779del , LRG_457t1:c.1777_1779del	NP_004110.2:p.Asp593del
NR_130706.1:n.1859_1861del
NR_130706.2:n.1843_1845del
ENST00000241453.11:c.1777_1779del	ENSP00000241453.7:p.Asp593del
ENST00000380987.2:c.1777_1779del	ENSP00000370374.2:p.Asp593del
XM_011535015.1:c.1720_1722del	XP_011533317.1:p.Asp574del
XM_011535015.2:c.1720_1722del	XP_011533317.1:p.Asp574del
XM_011535016.1:c.1252_1254del	XP_011533318.1:p.Asp418del
XM_011535017.1:c.1252_1254del	XP_011533319.1:p.Asp418del
XM_011535017.2:c.1252_1254del	XP_011533319.1:p.Asp418del
XM_011535018.1:c.1252_1254del	XP_011533320.1:p.Asp418del
XM_011535018.2:c.1252_1254del	XP_011533320.1:p.Asp418del
XM_017020486.1:c.1561_1563del	XP_016875975.1:p.Asp521del
XM_017020487.1:c.1252_1254del	XP_016875976.1:p.Asp418del
XM_017020488.1:c.898_900del	XP_016875977.1:p.Asp300del
XM_017020489.1:c.880_882del	XP_016875978.1:p.Asp294del