Canonical Allele Identifier: CA2080793316

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034212T= , CM000675.2:g.28034212T=	GRCh38
NC_000013.10:g.28608349T= , CM000675.1:g.28608349T=	GRCh37
NC_000013.9:g.27506349T=	NCBI36
NG_007066.1:g.71357A= , LRG_457:g.71357A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1707A= MANE Select	ENSP00000241453.7:p.Gln569=
ENST00000241453.11:c.1707A=	ENSP00000241453.7:p.Gln569=
ENST00000380987.2:c.1707A=	ENSP00000370374.2:p.Gln569=
NM_004119.2:c.1707A= , LRG_457t1:c.1707A=	NP_004110.2:p.Gln569=
NR_130706.1:n.1789A=
XM_011535015.1:c.1650A=	XP_011533317.1:p.Gln550=
XM_011535016.1:c.1182A=	XP_011533318.1:p.Gln394=
XM_011535017.1:c.1182A=	XP_011533319.1:p.Gln394=
XM_011535018.1:c.1182A=	XP_011533320.1:p.Gln394=
XM_011535015.2:c.1650A=	XP_011533317.1:p.Gln550=
XM_011535017.2:c.1182A=	XP_011533319.1:p.Gln394=
XM_011535018.2:c.1182A=	XP_011533320.1:p.Gln394=
XM_017020486.1:c.1491A=	XP_016875975.1:p.Gln497=
XM_017020487.1:c.1182A=	XP_016875976.1:p.Gln394=
XM_017020488.1:c.828A=	XP_016875977.1:p.Gln276=
XM_017020489.1:c.810A=	XP_016875978.1:p.Gln270=
NM_004119.3:c.1707A= MANE Select	NP_004110.2:p.Gln569=
NR_130706.2:n.1773A=