Canonical Allele Identifier: CA2080790613

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028238T= , CM000675.2:g.28028238T=	GRCh38
NC_000013.10:g.28602375T= , CM000675.1:g.28602375T=	GRCh37
NC_000013.9:g.27500375T=	NCBI36
NG_007066.1:g.77331A= , LRG_457:g.77331A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1993A= MANE Select	ENSP00000241453.7:p.Met665=
ENST00000241453.11:c.1993A=	ENSP00000241453.7:p.Met665=
ENST00000380987.2:c.1993A=	ENSP00000370374.2:p.Met665=
NM_004119.2:c.1993A= , LRG_457t1:c.1993A=	NP_004110.2:p.Met665=
NR_130706.1:n.2075A=
XM_011535015.1:c.1936A=	XP_011533317.1:p.Met646=
XM_011535016.1:c.1468A=	XP_011533318.1:p.Met490=
XM_011535017.1:c.1468A=	XP_011533319.1:p.Met490=
XM_011535018.1:c.1468A=	XP_011533320.1:p.Met490=
XM_011535015.2:c.1936A=	XP_011533317.1:p.Met646=
XM_011535017.2:c.1468A=	XP_011533319.1:p.Met490=
XM_011535018.2:c.1468A=	XP_011533320.1:p.Met490=
XM_017020486.1:c.1777A=	XP_016875975.1:p.Met593=
XM_017020487.1:c.1468A=	XP_016875976.1:p.Met490=
XM_017020488.1:c.1114A=	XP_016875977.1:p.Met372=
XM_017020489.1:c.1096A=	XP_016875978.1:p.Met366=
NM_004119.3:c.1993A= MANE Select	NP_004110.2:p.Met665=
NR_130706.2:n.2059A=