Canonical Allele Identifier: CA2080781569

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018553C= , CM000675.2:g.28018553C=	GRCh38
NC_000013.10:g.28592690C= , CM000675.1:g.28592690C=	GRCh37
NC_000013.9:g.27490690C=	NCBI36
NG_007066.1:g.87016G= , LRG_457:g.87016G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2455G= MANE Select	ENSP00000241453.7:p.Val819=
ENST00000241453.11:c.2455G=	ENSP00000241453.7:p.Val819=
ENST00000380987.2:c.*367G=	ENSP00000370374.2:n.*367G=
NM_004119.2:c.2455G= , LRG_457t1:c.2455G=	NP_004110.2:p.Val819=
NR_130706.1:n.2669G=
XM_011535015.1:c.2398G=	XP_011533317.1:p.Val800=
XM_011535016.1:c.1930G=	XP_011533318.1:p.Val644=
XM_011535017.1:c.1930G=	XP_011533319.1:p.Val644=
XM_011535018.1:c.1930G=	XP_011533320.1:p.Val644=
XM_011535015.2:c.2398G=	XP_011533317.1:p.Val800=
XM_011535017.2:c.1930G=	XP_011533319.1:p.Val644=
XM_011535018.2:c.1930G=	XP_011533320.1:p.Val644=
XM_017020486.1:c.2239G=	XP_016875975.1:p.Val747=
XM_017020487.1:c.1930G=	XP_016875976.1:p.Val644=
XM_017020488.1:c.1576G=	XP_016875977.1:p.Val526=
XM_017020489.1:c.1558G=	XP_016875978.1:p.Val520=
NM_004119.3:c.2455G= MANE Select	NP_004110.2:p.Val819=
NR_130706.2:n.2653G=