Canonical Allele Identifier: CA2080781552

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018537A= , CM000675.2:g.28018537A=	GRCh38
NC_000013.10:g.28592674A= , CM000675.1:g.28592674A=	GRCh37
NC_000013.9:g.27490674A=	NCBI36
NG_007066.1:g.87032T= , LRG_457:g.87032T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2471T= MANE Select	ENSP00000241453.7:p.Val824=
ENST00000241453.11:c.2471T=	ENSP00000241453.7:p.Val824=
ENST00000380987.2:c.*383T=	ENSP00000370374.2:n.*383T=
NM_004119.2:c.2471T= , LRG_457t1:c.2471T=	NP_004110.2:p.Val824=
NR_130706.1:n.2685T=
XM_011535015.1:c.2414T=	XP_011533317.1:p.Val805=
XM_011535016.1:c.1946T=	XP_011533318.1:p.Val649=
XM_011535017.1:c.1946T=	XP_011533319.1:p.Val649=
XM_011535018.1:c.1946T=	XP_011533320.1:p.Val649=
XM_011535015.2:c.2414T=	XP_011533317.1:p.Val805=
XM_011535017.2:c.1946T=	XP_011533319.1:p.Val649=
XM_011535018.2:c.1946T=	XP_011533320.1:p.Val649=
XM_017020486.1:c.2255T=	XP_016875975.1:p.Val752=
XM_017020487.1:c.1946T=	XP_016875976.1:p.Val649=
XM_017020488.1:c.1592T=	XP_016875977.1:p.Val531=
XM_017020489.1:c.1574T=	XP_016875978.1:p.Val525=
NM_004119.3:c.2471T= MANE Select	NP_004110.2:p.Val824=
NR_130706.2:n.2669T=