Canonical Allele Identifier: CA6928787

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28049388G>A , CM000675.2:g.28049388G>A	GRCh38
NC_000013.10:g.28623525G>A , CM000675.1:g.28623525G>A	GRCh37
NC_000013.9:g.27521525G>A	NCBI36
NG_007066.1:g.56181C>T , LRG_457:g.56181C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1032C>T MANE Select	ENSP00000241453.7:p.Ile344=
ENST00000241453.11:c.1032C>T	ENSP00000241453.7:p.Ile344=
ENST00000380987.2:c.1032C>T	ENSP00000370374.2:p.Ile344=
NM_004119.2:c.1032C>T , LRG_457t1:c.1032C>T	NP_004110.2:p.Ile344=
NR_130706.1:n.1114C>T
XM_011535015.1:c.975C>T	XP_011533317.1:p.Ile325=
XM_011535016.1:c.507C>T	XP_011533318.1:p.Ile169=
XM_011535017.1:c.507C>T	XP_011533319.1:p.Ile169=
XM_011535018.1:c.507C>T	XP_011533320.1:p.Ile169=
XM_011535015.2:c.975C>T	XP_011533317.1:p.Ile325=
XM_011535017.2:c.507C>T	XP_011533319.1:p.Ile169=
XM_011535018.2:c.507C>T	XP_011533320.1:p.Ile169=
XM_017020486.1:c.816C>T	XP_016875975.1:p.Ile272=
XM_017020487.1:c.507C>T	XP_016875976.1:p.Ile169=
XM_017020488.1:c.153C>T	XP_016875977.1:p.Ile51=
XM_017020489.1:c.135C>T	XP_016875978.1:p.Ile45=
NM_004119.3:c.1032C>T MANE Select	NP_004110.2:p.Ile344=
NR_130706.2:n.1098C>T