Canonical Allele Identifier: CA387641102

Gene: FLT3

Linked Data

• dbSNP Id: rs2137676110
• MyVariant Identifiers: chr13:g.28608337T>A (hg19) ; chr13:g.28034200T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034200T>A , CM000675.2:g.28034200T>A	GRCh38
NC_000013.10:g.28608337T>A , CM000675.1:g.28608337T>A	GRCh37
NC_000013.9:g.27506337T>A	NCBI36
NG_007066.1:g.71369A>T , LRG_457:g.71369A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1719A>T MANE Select	ENSP00000241453.7:p.Glu573Asp
ENST00000241453.11:c.1719A>T	ENSP00000241453.7:p.Glu573Asp
ENST00000380987.2:c.1719A>T	ENSP00000370374.2:p.Glu573Asp
NM_004119.2:c.1719A>T , LRG_457t1:c.1719A>T	NP_004110.2:p.Glu573Asp
NR_130706.1:n.1801A>T
XM_011535015.1:c.1662A>T	XP_011533317.1:p.Glu554Asp
XM_011535016.1:c.1194A>T	XP_011533318.1:p.Glu398Asp
XM_011535017.1:c.1194A>T	XP_011533319.1:p.Glu398Asp
XM_011535018.1:c.1194A>T	XP_011533320.1:p.Glu398Asp
XM_011535015.2:c.1662A>T	XP_011533317.1:p.Glu554Asp
XM_011535017.2:c.1194A>T	XP_011533319.1:p.Glu398Asp
XM_011535018.2:c.1194A>T	XP_011533320.1:p.Glu398Asp
XM_017020486.1:c.1503A>T	XP_016875975.1:p.Glu501Asp
XM_017020487.1:c.1194A>T	XP_016875976.1:p.Glu398Asp
XM_017020488.1:c.840A>T	XP_016875977.1:p.Glu280Asp
XM_017020489.1:c.822A>T	XP_016875978.1:p.Glu274Asp
NM_004119.3:c.1719A>T MANE Select	NP_004110.2:p.Glu573Asp
NR_130706.2:n.1785A>T