Canonical Allele Identifier: CA2080781611

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018569G= , CM000675.2:g.28018569G=	GRCh38
NC_000013.10:g.28592706G= , CM000675.1:g.28592706G=	GRCh37
NC_000013.9:g.27490706G=	NCBI36
NG_007066.1:g.87000C= , LRG_457:g.87000C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2439C= MANE Select	ENSP00000241453.7:p.Ala813=
ENST00000241453.11:c.2439C=	ENSP00000241453.7:p.Ala813=
ENST00000380987.2:c.*351C=	ENSP00000370374.2:n.*351C=
NM_004119.2:c.2439C= , LRG_457t1:c.2439C=	NP_004110.2:p.Ala813=
NR_130706.1:n.2653C=
XM_011535015.1:c.2382C=	XP_011533317.1:p.Ala794=
XM_011535016.1:c.1914C=	XP_011533318.1:p.Ala638=
XM_011535017.1:c.1914C=	XP_011533319.1:p.Ala638=
XM_011535018.1:c.1914C=	XP_011533320.1:p.Ala638=
XM_011535015.2:c.2382C=	XP_011533317.1:p.Ala794=
XM_011535017.2:c.1914C=	XP_011533319.1:p.Ala638=
XM_011535018.2:c.1914C=	XP_011533320.1:p.Ala638=
XM_017020486.1:c.2223C=	XP_016875975.1:p.Ala741=
XM_017020487.1:c.1914C=	XP_016875976.1:p.Ala638=
XM_017020488.1:c.1560C=	XP_016875977.1:p.Ala520=
XM_017020489.1:c.1542C=	XP_016875978.1:p.Ala514=
NM_004119.3:c.2439C= MANE Select	NP_004110.2:p.Ala813=
NR_130706.2:n.2637C=