Canonical Allele Identifier: CA2080781464

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018502T= , CM000675.2:g.28018502T=	GRCh38
NC_000013.10:g.28592639T= , CM000675.1:g.28592639T=	GRCh37
NC_000013.9:g.27490639T=	NCBI36
NG_007066.1:g.87067A= , LRG_457:g.87067A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2506A= MANE Select	ENSP00000241453.7:p.Ile836=
ENST00000241453.11:c.2506A=	ENSP00000241453.7:p.Ile836=
ENST00000380987.2:c.*418A=	ENSP00000370374.2:n.*418A=
NM_004119.2:c.2506A= , LRG_457t1:c.2506A=	NP_004110.2:p.Ile836=
NR_130706.1:n.2720A=
XM_011535015.1:c.2449A=	XP_011533317.1:p.Ile817=
XM_011535016.1:c.1981A=	XP_011533318.1:p.Ile661=
XM_011535017.1:c.1981A=	XP_011533319.1:p.Ile661=
XM_011535018.1:c.1981A=	XP_011533320.1:p.Ile661=
XM_011535015.2:c.2449A=	XP_011533317.1:p.Ile817=
XM_011535017.2:c.1981A=	XP_011533319.1:p.Ile661=
XM_011535018.2:c.1981A=	XP_011533320.1:p.Ile661=
XM_017020486.1:c.2290A=	XP_016875975.1:p.Ile764=
XM_017020487.1:c.1981A=	XP_016875976.1:p.Ile661=
XM_017020488.1:c.1627A=	XP_016875977.1:p.Ile543=
XM_017020489.1:c.1609A=	XP_016875978.1:p.Ile537=
NM_004119.3:c.2506A= MANE Select	NP_004110.2:p.Ile836=
NR_130706.2:n.2704A=