Canonical Allele Identifier: CA2080781631

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018587A= , CM000675.2:g.28018587A=	GRCh38
NC_000013.10:g.28592724A= , CM000675.1:g.28592724A=	GRCh37
NC_000013.9:g.27490724A=	NCBI36
NG_007066.1:g.86982T= , LRG_457:g.86982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2421T= MANE Select	ENSP00000241453.7:p.Cys807=
ENST00000241453.11:c.2421T=	ENSP00000241453.7:p.Cys807=
ENST00000380987.2:c.*333T=	ENSP00000370374.2:n.*333T=
NM_004119.2:c.2421T= , LRG_457t1:c.2421T=	NP_004110.2:p.Cys807=
NR_130706.1:n.2635T=
XM_011535015.1:c.2364T=	XP_011533317.1:p.Cys788=
XM_011535016.1:c.1896T=	XP_011533318.1:p.Cys632=
XM_011535017.1:c.1896T=	XP_011533319.1:p.Cys632=
XM_011535018.1:c.1896T=	XP_011533320.1:p.Cys632=
XM_011535015.2:c.2364T=	XP_011533317.1:p.Cys788=
XM_011535017.2:c.1896T=	XP_011533319.1:p.Cys632=
XM_011535018.2:c.1896T=	XP_011533320.1:p.Cys632=
XM_017020486.1:c.2205T=	XP_016875975.1:p.Cys735=
XM_017020487.1:c.1896T=	XP_016875976.1:p.Cys632=
XM_017020488.1:c.1542T=	XP_016875977.1:p.Cys514=
XM_017020489.1:c.1524T=	XP_016875978.1:p.Cys508=
NM_004119.3:c.2421T= MANE Select	NP_004110.2:p.Cys807=
NR_130706.2:n.2619T=