Canonical Allele Identifier: CA6928272

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28015689C>T , CM000675.2:g.28015689C>T	GRCh38
NC_000013.10:g.28589826C>T , CM000675.1:g.28589826C>T	GRCh37
NC_000013.9:g.27487826C>T	NCBI36
NG_007066.1:g.89880G>A , LRG_457:g.89880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2554G>A MANE Select	ENSP00000241453.7:p.Val852Ile
ENST00000241453.11:c.2554G>A	ENSP00000241453.7:p.Val852Ile
ENST00000380987.2:c.*466G>A	ENSP00000370374.2:n.*466G>A
NM_004119.2:c.2554G>A , LRG_457t1:c.2554G>A	NP_004110.2:p.Val852Ile
NR_130706.1:n.2768G>A
XM_011535015.1:c.2497G>A	XP_011533317.1:p.Val833Ile
XM_011535016.1:c.2029G>A	XP_011533318.1:p.Val677Ile
XM_011535017.1:c.2029G>A	XP_011533319.1:p.Val677Ile
XM_011535018.1:c.2029G>A	XP_011533320.1:p.Val677Ile
XM_011535015.2:c.2497G>A	XP_011533317.1:p.Val833Ile
XM_011535017.2:c.2029G>A	XP_011533319.1:p.Val677Ile
XM_011535018.2:c.2029G>A	XP_011533320.1:p.Val677Ile
XM_017020486.1:c.2338G>A	XP_016875975.1:p.Val780Ile
XM_017020487.1:c.2029G>A	XP_016875976.1:p.Val677Ile
XM_017020488.1:c.1675G>A	XP_016875977.1:p.Val559Ile
XM_017020489.1:c.1657G>A	XP_016875978.1:p.Val553Ile
NM_004119.3:c.2554G>A MANE Select	NP_004110.2:p.Val852Ile
NR_130706.2:n.2752G>A