Canonical Allele Identifier: CA2080790188

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28027222A= , CM000675.2:g.28027222A=	GRCh38
NC_000013.10:g.28601359A= , CM000675.1:g.28601359A=	GRCh37
NC_000013.9:g.27499359A=	NCBI36
NG_007066.1:g.78347T= , LRG_457:g.78347T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004119.3:c.2073T= MANE Select	NP_004110.2:p.Phe691=
ENST00000241453.12:c.2073T= MANE Select	ENSP00000241453.7:p.Phe691=
NM_004119.2:c.2073T= , LRG_457t1:c.2073T=	NP_004110.2:p.Phe691=
NR_130706.1:n.2155T=
NR_130706.2:n.2139T=
ENST00000241453.11:c.2073T=	ENSP00000241453.7:p.Phe691=
ENST00000380987.2:c.2073T=	ENSP00000370374.2:p.Phe691=
XM_011535015.1:c.2016T=	XP_011533317.1:p.Phe672=
XM_011535015.2:c.2016T=	XP_011533317.1:p.Phe672=
XM_011535016.1:c.1548T=	XP_011533318.1:p.Phe516=
XM_011535017.1:c.1548T=	XP_011533319.1:p.Phe516=
XM_011535017.2:c.1548T=	XP_011533319.1:p.Phe516=
XM_011535018.1:c.1548T=	XP_011533320.1:p.Phe516=
XM_011535018.2:c.1548T=	XP_011533320.1:p.Phe516=
XM_017020486.1:c.1857T=	XP_016875975.1:p.Phe619=
XM_017020487.1:c.1548T=	XP_016875976.1:p.Phe516=
XM_017020488.1:c.1194T=	XP_016875977.1:p.Phe398=
XM_017020489.1:c.1176T=	XP_016875978.1:p.Phe392=