Canonical Allele Identifier: CA2080781409

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018493C= , CM000675.2:g.28018493C=	GRCh38
NC_000013.10:g.28592630C= , CM000675.1:g.28592630C=	GRCh37
NC_000013.9:g.27490630C=	NCBI36
NG_007066.1:g.87076G= , LRG_457:g.87076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2515G= MANE Select	ENSP00000241453.7:p.Asp839=
ENST00000241453.11:c.2515G=	ENSP00000241453.7:p.Asp839=
ENST00000380987.2:c.*427G=	ENSP00000370374.2:n.*427G=
NM_004119.2:c.2515G= , LRG_457t1:c.2515G=	NP_004110.2:p.Asp839=
NR_130706.1:n.2729G=
XM_011535015.1:c.2458G=	XP_011533317.1:p.Asp820=
XM_011535016.1:c.1990G=	XP_011533318.1:p.Asp664=
XM_011535017.1:c.1990G=	XP_011533319.1:p.Asp664=
XM_011535018.1:c.1990G=	XP_011533320.1:p.Asp664=
XM_011535015.2:c.2458G=	XP_011533317.1:p.Asp820=
XM_011535017.2:c.1990G=	XP_011533319.1:p.Asp664=
XM_011535018.2:c.1990G=	XP_011533320.1:p.Asp664=
XM_017020486.1:c.2299G=	XP_016875975.1:p.Asp767=
XM_017020487.1:c.1990G=	XP_016875976.1:p.Asp664=
XM_017020488.1:c.1636G=	XP_016875977.1:p.Asp546=
XM_017020489.1:c.1618G=	XP_016875978.1:p.Asp540=
NM_004119.3:c.2515G= MANE Select	NP_004110.2:p.Asp839=
NR_130706.2:n.2713G=