Canonical Allele Identifier: CA2080781531

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018527T= , CM000675.2:g.28018527T=	GRCh38
NC_000013.10:g.28592664T= , CM000675.1:g.28592664T=	GRCh37
NC_000013.9:g.27490664T=	NCBI36
NG_007066.1:g.87042A= , LRG_457:g.87042A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2481A= MANE Select	ENSP00000241453.7:p.Ile827=
ENST00000241453.11:c.2481A=	ENSP00000241453.7:p.Ile827=
ENST00000380987.2:c.*393A=	ENSP00000370374.2:n.*393A=
NM_004119.2:c.2481A= , LRG_457t1:c.2481A=	NP_004110.2:p.Ile827=
NR_130706.1:n.2695A=
XM_011535015.1:c.2424A=	XP_011533317.1:p.Ile808=
XM_011535016.1:c.1956A=	XP_011533318.1:p.Ile652=
XM_011535017.1:c.1956A=	XP_011533319.1:p.Ile652=
XM_011535018.1:c.1956A=	XP_011533320.1:p.Ile652=
XM_011535015.2:c.2424A=	XP_011533317.1:p.Ile808=
XM_011535017.2:c.1956A=	XP_011533319.1:p.Ile652=
XM_011535018.2:c.1956A=	XP_011533320.1:p.Ile652=
XM_017020486.1:c.2265A=	XP_016875975.1:p.Ile755=
XM_017020487.1:c.1956A=	XP_016875976.1:p.Ile652=
XM_017020488.1:c.1602A=	XP_016875977.1:p.Ile534=
XM_017020489.1:c.1584A=	XP_016875978.1:p.Ile528=
NM_004119.3:c.2481A= MANE Select	NP_004110.2:p.Ile827=
NR_130706.2:n.2679A=