Canonical Allele Identifier: CA159861

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28048407T>A , CM000675.2:g.28048407T>A	GRCh38
NC_000013.10:g.28622544T>A , CM000675.1:g.28622544T>A	GRCh37
NC_000013.9:g.27520544T>A	NCBI36
NG_007066.1:g.57162A>T , LRG_457:g.57162A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1073A>T MANE Select	ENSP00000241453.7:p.Asp358Val
ENST00000241453.11:c.1073A>T	ENSP00000241453.7:p.Asp358Val
ENST00000380987.2:c.1073A>T	ENSP00000370374.2:p.Asp358Val
NM_004119.2:c.1073A>T , LRG_457t1:c.1073A>T	NP_004110.2:p.Asp358Val
NR_130706.1:n.1155A>T
XM_011535015.1:c.1016A>T	XP_011533317.1:p.Asp339Val
XM_011535016.1:c.548A>T	XP_011533318.1:p.Asp183Val
XM_011535017.1:c.548A>T	XP_011533319.1:p.Asp183Val
XM_011535018.1:c.548A>T	XP_011533320.1:p.Asp183Val
XM_011535015.2:c.1016A>T	XP_011533317.1:p.Asp339Val
XM_011535017.2:c.548A>T	XP_011533319.1:p.Asp183Val
XM_011535018.2:c.548A>T	XP_011533320.1:p.Asp183Val
XM_017020486.1:c.857A>T	XP_016875975.1:p.Asp286Val
XM_017020487.1:c.548A>T	XP_016875976.1:p.Asp183Val
XM_017020488.1:c.194A>T	XP_016875977.1:p.Asp65Val
XM_017020489.1:c.176A>T	XP_016875978.1:p.Asp59Val
NM_004119.3:c.1073A>T MANE Select	NP_004110.2:p.Asp358Val
NR_130706.2:n.1139A>T