Canonical Allele Identifier: CA2080781669

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018620C= , CM000675.2:g.28018620C=	GRCh38
NC_000013.10:g.28592757C= , CM000675.1:g.28592757C=	GRCh37
NC_000013.9:g.27490757C=	NCBI36
NG_007066.1:g.86949G= , LRG_457:g.86949G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-31G= MANE Select	ENSP00000241453.7:n.2419-31G=
ENST00000241453.11:c.2419-31G=	ENSP00000241453.7:n.2419-31G=
ENST00000380987.2:c.*331-31G=	ENSP00000370374.2:n.*331-31G=
NM_004119.2:c.2419-31G= , LRG_457t1:c.2419-31G=	NP_004110.2:n.2419-31G=
NR_130706.1:n.2633-31G=
XM_011535015.1:c.2362-31G=	XP_011533317.1:n.2362-31G=
XM_011535016.1:c.1894-31G=	XP_011533318.1:n.1894-31G=
XM_011535017.1:c.1894-31G=	XP_011533319.1:n.1894-31G=
XM_011535018.1:c.1894-31G=	XP_011533320.1:n.1894-31G=
XM_011535015.2:c.2362-31G=	XP_011533317.1:n.2362-31G=
XM_011535017.2:c.1894-31G=	XP_011533319.1:n.1894-31G=
XM_011535018.2:c.1894-31G=	XP_011533320.1:n.1894-31G=
XM_017020486.1:c.2203-31G=	XP_016875975.1:n.2203-31G=
XM_017020487.1:c.1894-31G=	XP_016875976.1:n.1894-31G=
XM_017020488.1:c.1540-31G=	XP_016875977.1:n.1540-31G=
XM_017020489.1:c.1522-31G=	XP_016875978.1:n.1522-31G=
NM_004119.3:c.2419-31G= MANE Select	NP_004110.2:n.2419-31G=
NR_130706.2:n.2617-31G=