Canonical Allele Identifier: CA2080781903

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018884G= , CM000675.2:g.28018884G=	GRCh38
NC_000013.10:g.28593021G= , CM000675.1:g.28593021G=	GRCh37
NC_000013.9:g.27491021G=	NCBI36
NG_007066.1:g.86685C= , LRG_457:g.86685C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-295C= MANE Select	ENSP00000241453.7:n.2419-295C=
ENST00000241453.11:c.2419-295C=	ENSP00000241453.7:n.2419-295C=
ENST00000380987.2:c.*331-295C=	ENSP00000370374.2:n.*331-295C=
NM_004119.2:c.2419-295C= , LRG_457t1:c.2419-295C=	NP_004110.2:n.2419-295C=
NR_130706.1:n.2633-295C=
XM_011535015.1:c.2362-295C=	XP_011533317.1:n.2362-295C=
XM_011535016.1:c.1894-295C=	XP_011533318.1:n.1894-295C=
XM_011535017.1:c.1894-295C=	XP_011533319.1:n.1894-295C=
XM_011535018.1:c.1894-295C=	XP_011533320.1:n.1894-295C=
XM_011535015.2:c.2362-295C=	XP_011533317.1:n.2362-295C=
XM_011535017.2:c.1894-295C=	XP_011533319.1:n.1894-295C=
XM_011535018.2:c.1894-295C=	XP_011533320.1:n.1894-295C=
XM_017020486.1:c.2203-295C=	XP_016875975.1:n.2203-295C=
XM_017020487.1:c.1894-295C=	XP_016875976.1:n.1894-295C=
XM_017020488.1:c.1540-295C=	XP_016875977.1:n.1540-295C=
XM_017020489.1:c.1522-295C=	XP_016875978.1:n.1522-295C=
NM_004119.3:c.2419-295C= MANE Select	NP_004110.2:n.2419-295C=
NR_130706.2:n.2617-295C=