Canonical Allele Identifier: CA2080780936

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28017990G= , CM000675.2:g.28017990G=	GRCh38
NC_000013.10:g.28592127G= , CM000675.1:g.28592127G=	GRCh37
NC_000013.9:g.27490127G=	NCBI36
NG_007066.1:g.87579C= , LRG_457:g.87579C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2541+477C= MANE Select	ENSP00000241453.7:n.2541+477C=
ENST00000241453.11:c.2541+477C=	ENSP00000241453.7:n.2541+477C=
ENST00000380987.2:c.*453+477C=	ENSP00000370374.2:n.*453+477C=
NM_004119.2:c.2541+477C= , LRG_457t1:c.2541+477C=	NP_004110.2:n.2541+477C=
NR_130706.1:n.2755+477C=
XM_011535015.1:c.2484+477C=	XP_011533317.1:n.2484+477C=
XM_011535016.1:c.2016+477C=	XP_011533318.1:n.2016+477C=
XM_011535017.1:c.2016+477C=	XP_011533319.1:n.2016+477C=
XM_011535018.1:c.2016+477C=	XP_011533320.1:n.2016+477C=
XM_011535015.2:c.2484+477C=	XP_011533317.1:n.2484+477C=
XM_011535017.2:c.2016+477C=	XP_011533319.1:n.2016+477C=
XM_011535018.2:c.2016+477C=	XP_011533320.1:n.2016+477C=
XM_017020486.1:c.2325+477C=	XP_016875975.1:n.2325+477C=
XM_017020487.1:c.2016+477C=	XP_016875976.1:n.2016+477C=
XM_017020488.1:c.1662+477C=	XP_016875977.1:n.1662+477C=
XM_017020489.1:c.1644+477C=	XP_016875978.1:n.1644+477C=
NM_004119.3:c.2541+477C= MANE Select	NP_004110.2:n.2541+477C=
NR_130706.2:n.2739+477C=