Canonical Allele Identifier: CA2080781561

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018545G= , CM000675.2:g.28018545G=	GRCh38
NC_000013.10:g.28592682G= , CM000675.1:g.28592682G=	GRCh37
NC_000013.9:g.27490682G=	NCBI36
NG_007066.1:g.87024C= , LRG_457:g.87024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2463C= MANE Select	ENSP00000241453.7:p.His821=
ENST00000241453.11:c.2463C=	ENSP00000241453.7:p.His821=
ENST00000380987.2:c.*375C=	ENSP00000370374.2:n.*375C=
NM_004119.2:c.2463C= , LRG_457t1:c.2463C=	NP_004110.2:p.His821=
NR_130706.1:n.2677C=
XM_011535015.1:c.2406C=	XP_011533317.1:p.His802=
XM_011535016.1:c.1938C=	XP_011533318.1:p.His646=
XM_011535017.1:c.1938C=	XP_011533319.1:p.His646=
XM_011535018.1:c.1938C=	XP_011533320.1:p.His646=
XM_011535015.2:c.2406C=	XP_011533317.1:p.His802=
XM_011535017.2:c.1938C=	XP_011533319.1:p.His646=
XM_011535018.2:c.1938C=	XP_011533320.1:p.His646=
XM_017020486.1:c.2247C=	XP_016875975.1:p.His749=
XM_017020487.1:c.1938C=	XP_016875976.1:p.His646=
XM_017020488.1:c.1584C=	XP_016875977.1:p.His528=
XM_017020489.1:c.1566C=	XP_016875978.1:p.His522=
NM_004119.3:c.2463C= MANE Select	NP_004110.2:p.His821=
NR_130706.2:n.2661C=