Canonical Allele Identifier: CA2080781376

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018485G= , CM000675.2:g.28018485G=	GRCh38
NC_000013.10:g.28592622G= , CM000675.1:g.28592622G=	GRCh37
NC_000013.9:g.27490622G=	NCBI36
NG_007066.1:g.87084C= , LRG_457:g.87084C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2523C= MANE Select	ENSP00000241453.7:p.Asn841=
ENST00000241453.11:c.2523C=	ENSP00000241453.7:p.Asn841=
ENST00000380987.2:c.*435C=	ENSP00000370374.2:n.*435C=
NM_004119.2:c.2523C= , LRG_457t1:c.2523C=	NP_004110.2:p.Asn841=
NR_130706.1:n.2737C=
XM_011535015.1:c.2466C=	XP_011533317.1:p.Asn822=
XM_011535016.1:c.1998C=	XP_011533318.1:p.Asn666=
XM_011535017.1:c.1998C=	XP_011533319.1:p.Asn666=
XM_011535018.1:c.1998C=	XP_011533320.1:p.Asn666=
XM_011535015.2:c.2466C=	XP_011533317.1:p.Asn822=
XM_011535017.2:c.1998C=	XP_011533319.1:p.Asn666=
XM_011535018.2:c.1998C=	XP_011533320.1:p.Asn666=
XM_017020486.1:c.2307C=	XP_016875975.1:p.Asn769=
XM_017020487.1:c.1998C=	XP_016875976.1:p.Asn666=
XM_017020488.1:c.1644C=	XP_016875977.1:p.Asn548=
XM_017020489.1:c.1626C=	XP_016875978.1:p.Asn542=
NM_004119.3:c.2523C= MANE Select	NP_004110.2:p.Asn841=
NR_130706.2:n.2721C=