Canonical Allele Identifier: CA2080781548

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018535C= , CM000675.2:g.28018535C=	GRCh38
NC_000013.10:g.28592672C= , CM000675.1:g.28592672C=	GRCh37
NC_000013.9:g.27490672C=	NCBI36
NG_007066.1:g.87034G= , LRG_457:g.87034G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2473G= MANE Select	ENSP00000241453.7:p.Val825=
ENST00000241453.11:c.2473G=	ENSP00000241453.7:p.Val825=
ENST00000380987.2:c.*385G=	ENSP00000370374.2:n.*385G=
NM_004119.2:c.2473G= , LRG_457t1:c.2473G=	NP_004110.2:p.Val825=
NR_130706.1:n.2687G=
XM_011535015.1:c.2416G=	XP_011533317.1:p.Val806=
XM_011535016.1:c.1948G=	XP_011533318.1:p.Val650=
XM_011535017.1:c.1948G=	XP_011533319.1:p.Val650=
XM_011535018.1:c.1948G=	XP_011533320.1:p.Val650=
XM_011535015.2:c.2416G=	XP_011533317.1:p.Val806=
XM_011535017.2:c.1948G=	XP_011533319.1:p.Val650=
XM_011535018.2:c.1948G=	XP_011533320.1:p.Val650=
XM_017020486.1:c.2257G=	XP_016875975.1:p.Val753=
XM_017020487.1:c.1948G=	XP_016875976.1:p.Val650=
XM_017020488.1:c.1594G=	XP_016875977.1:p.Val532=
XM_017020489.1:c.1576G=	XP_016875978.1:p.Val526=
NM_004119.3:c.2473G= MANE Select	NP_004110.2:p.Val825=
NR_130706.2:n.2671G=