Canonical Allele Identifier: CA2080790588

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028171G= , CM000675.2:g.28028171G=	GRCh38
NC_000013.10:g.28602308G= , CM000675.1:g.28602308G=	GRCh37
NC_000013.9:g.27500308G=	NCBI36
NG_007066.1:g.77398C= , LRG_457:g.77398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+7C= MANE Select	ENSP00000241453.7:n.2053+7C=
ENST00000241453.11:c.2053+7C=	ENSP00000241453.7:n.2053+7C=
ENST00000380987.2:c.2053+7C=	ENSP00000370374.2:n.2053+7C=
NM_004119.2:c.2053+7C= , LRG_457t1:c.2053+7C=	NP_004110.2:n.2053+7C=
NR_130706.1:n.2135+7C=
XM_011535015.1:c.1996+7C=	XP_011533317.1:n.1996+7C=
XM_011535016.1:c.1528+7C=	XP_011533318.1:n.1528+7C=
XM_011535017.1:c.1528+7C=	XP_011533319.1:n.1528+7C=
XM_011535018.1:c.1528+7C=	XP_011533320.1:n.1528+7C=
XM_011535015.2:c.1996+7C=	XP_011533317.1:n.1996+7C=
XM_011535017.2:c.1528+7C=	XP_011533319.1:n.1528+7C=
XM_011535018.2:c.1528+7C=	XP_011533320.1:n.1528+7C=
XM_017020486.1:c.1837+7C=	XP_016875975.1:n.1837+7C=
XM_017020487.1:c.1528+7C=	XP_016875976.1:n.1528+7C=
XM_017020488.1:c.1174+7C=	XP_016875977.1:n.1174+7C=
XM_017020489.1:c.1156+7C=	XP_016875978.1:n.1156+7C=
NM_004119.3:c.2053+7C= MANE Select	NP_004110.2:n.2053+7C=
NR_130706.2:n.2119+7C=