Canonical Allele Identifier: CA2080793249

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034149G= , CM000675.2:g.28034149G=	GRCh38
NC_000013.10:g.28608286G= , CM000675.1:g.28608286G=	GRCh37
NC_000013.9:g.27506286G=	NCBI36
NG_007066.1:g.71420C= , LRG_457:g.71420C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1770C= MANE Select	ENSP00000241453.7:p.Phe590=
ENST00000241453.11:c.1770C=	ENSP00000241453.7:p.Phe590=
ENST00000380987.2:c.1770C=	ENSP00000370374.2:p.Phe590=
NM_004119.2:c.1770C= , LRG_457t1:c.1770C=	NP_004110.2:p.Phe590=
NR_130706.1:n.1852C=
XM_011535015.1:c.1713C=	XP_011533317.1:p.Phe571=
XM_011535016.1:c.1245C=	XP_011533318.1:p.Phe415=
XM_011535017.1:c.1245C=	XP_011533319.1:p.Phe415=
XM_011535018.1:c.1245C=	XP_011533320.1:p.Phe415=
XM_011535015.2:c.1713C=	XP_011533317.1:p.Phe571=
XM_011535017.2:c.1245C=	XP_011533319.1:p.Phe415=
XM_011535018.2:c.1245C=	XP_011533320.1:p.Phe415=
XM_017020486.1:c.1554C=	XP_016875975.1:p.Phe518=
XM_017020487.1:c.1245C=	XP_016875976.1:p.Phe415=
XM_017020488.1:c.891C=	XP_016875977.1:p.Phe297=
XM_017020489.1:c.873C=	XP_016875978.1:p.Phe291=
NM_004119.3:c.1770C= MANE Select	NP_004110.2:p.Phe590=
NR_130706.2:n.1836C=