Canonical Allele Identifier: CA2080790587

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028169G= , CM000675.2:g.28028169G=	GRCh38
NC_000013.10:g.28602306G= , CM000675.1:g.28602306G=	GRCh37
NC_000013.9:g.27500306G=	NCBI36
NG_007066.1:g.77400C= , LRG_457:g.77400C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+9C= MANE Select	ENSP00000241453.7:n.2053+9C=
ENST00000241453.11:c.2053+9C=	ENSP00000241453.7:n.2053+9C=
ENST00000380987.2:c.2053+9C=	ENSP00000370374.2:n.2053+9C=
NM_004119.2:c.2053+9C= , LRG_457t1:c.2053+9C=	NP_004110.2:n.2053+9C=
NR_130706.1:n.2135+9C=
XM_011535015.1:c.1996+9C=	XP_011533317.1:n.1996+9C=
XM_011535016.1:c.1528+9C=	XP_011533318.1:n.1528+9C=
XM_011535017.1:c.1528+9C=	XP_011533319.1:n.1528+9C=
XM_011535018.1:c.1528+9C=	XP_011533320.1:n.1528+9C=
XM_011535015.2:c.1996+9C=	XP_011533317.1:n.1996+9C=
XM_011535017.2:c.1528+9C=	XP_011533319.1:n.1528+9C=
XM_011535018.2:c.1528+9C=	XP_011533320.1:n.1528+9C=
XM_017020486.1:c.1837+9C=	XP_016875975.1:n.1837+9C=
XM_017020487.1:c.1528+9C=	XP_016875976.1:n.1528+9C=
XM_017020488.1:c.1174+9C=	XP_016875977.1:n.1174+9C=
XM_017020489.1:c.1156+9C=	XP_016875978.1:n.1156+9C=
NM_004119.3:c.2053+9C= MANE Select	NP_004110.2:n.2053+9C=
NR_130706.2:n.2119+9C=