Canonical Allele Identifier: CA2080781483

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018503A= , CM000675.2:g.28018503A=	GRCh38
NC_000013.10:g.28592640A= , CM000675.1:g.28592640A=	GRCh37
NC_000013.9:g.27490640A=	NCBI36
NG_007066.1:g.87066T= , LRG_457:g.87066T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2505T= MANE Select	ENSP00000241453.7:p.Asp835=
ENST00000241453.11:c.2505T=	ENSP00000241453.7:p.Asp835=
ENST00000380987.2:c.*417T=	ENSP00000370374.2:n.*417T=
NM_004119.2:c.2505T= , LRG_457t1:c.2505T=	NP_004110.2:p.Asp835=
NR_130706.1:n.2719T=
XM_011535015.1:c.2448T=	XP_011533317.1:p.Asp816=
XM_011535016.1:c.1980T=	XP_011533318.1:p.Asp660=
XM_011535017.1:c.1980T=	XP_011533319.1:p.Asp660=
XM_011535018.1:c.1980T=	XP_011533320.1:p.Asp660=
XM_011535015.2:c.2448T=	XP_011533317.1:p.Asp816=
XM_011535017.2:c.1980T=	XP_011533319.1:p.Asp660=
XM_011535018.2:c.1980T=	XP_011533320.1:p.Asp660=
XM_017020486.1:c.2289T=	XP_016875975.1:p.Asp763=
XM_017020487.1:c.1980T=	XP_016875976.1:p.Asp660=
XM_017020488.1:c.1626T=	XP_016875977.1:p.Asp542=
XM_017020489.1:c.1608T=	XP_016875978.1:p.Asp536=
NM_004119.3:c.2505T= MANE Select	NP_004110.2:p.Asp835=
NR_130706.2:n.2703T=