Canonical Allele Identifier: CA2080790607

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028218G= , CM000675.2:g.28028218G=	GRCh38
NC_000013.10:g.28602355G= , CM000675.1:g.28602355G=	GRCh37
NC_000013.9:g.27500355G=	NCBI36
NG_007066.1:g.77351C= , LRG_457:g.77351C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2013C= MANE Select	ENSP00000241453.7:p.His671=
ENST00000241453.11:c.2013C=	ENSP00000241453.7:p.His671=
ENST00000380987.2:c.2013C=	ENSP00000370374.2:p.His671=
NM_004119.2:c.2013C= , LRG_457t1:c.2013C=	NP_004110.2:p.His671=
NR_130706.1:n.2095C=
XM_011535015.1:c.1956C=	XP_011533317.1:p.His652=
XM_011535016.1:c.1488C=	XP_011533318.1:p.His496=
XM_011535017.1:c.1488C=	XP_011533319.1:p.His496=
XM_011535018.1:c.1488C=	XP_011533320.1:p.His496=
XM_011535015.2:c.1956C=	XP_011533317.1:p.His652=
XM_011535017.2:c.1488C=	XP_011533319.1:p.His496=
XM_011535018.2:c.1488C=	XP_011533320.1:p.His496=
XM_017020486.1:c.1797C=	XP_016875975.1:p.His599=
XM_017020487.1:c.1488C=	XP_016875976.1:p.His496=
XM_017020488.1:c.1134C=	XP_016875977.1:p.His378=
XM_017020489.1:c.1116C=	XP_016875978.1:p.His372=
NM_004119.3:c.2013C= MANE Select	NP_004110.2:p.His671=
NR_130706.2:n.2079C=