Canonical Allele Identifier: CA2080790606

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028217C= , CM000675.2:g.28028217C=	GRCh38
NC_000013.10:g.28602354C= , CM000675.1:g.28602354C=	GRCh37
NC_000013.9:g.27500354C=	NCBI36
NG_007066.1:g.77352G= , LRG_457:g.77352G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2014G= MANE Select	ENSP00000241453.7:p.Glu672=
ENST00000241453.11:c.2014G=	ENSP00000241453.7:p.Glu672=
ENST00000380987.2:c.2014G=	ENSP00000370374.2:p.Glu672=
NM_004119.2:c.2014G= , LRG_457t1:c.2014G=	NP_004110.2:p.Glu672=
NR_130706.1:n.2096G=
XM_011535015.1:c.1957G=	XP_011533317.1:p.Glu653=
XM_011535016.1:c.1489G=	XP_011533318.1:p.Glu497=
XM_011535017.1:c.1489G=	XP_011533319.1:p.Glu497=
XM_011535018.1:c.1489G=	XP_011533320.1:p.Glu497=
XM_011535015.2:c.1957G=	XP_011533317.1:p.Glu653=
XM_011535017.2:c.1489G=	XP_011533319.1:p.Glu497=
XM_011535018.2:c.1489G=	XP_011533320.1:p.Glu497=
XM_017020486.1:c.1798G=	XP_016875975.1:p.Glu600=
XM_017020487.1:c.1489G=	XP_016875976.1:p.Glu497=
XM_017020488.1:c.1135G=	XP_016875977.1:p.Glu379=
XM_017020489.1:c.1117G=	XP_016875978.1:p.Glu373=
NM_004119.3:c.2014G= MANE Select	NP_004110.2:p.Glu672=
NR_130706.2:n.2080G=