Canonical Allele Identifier: CA387650231

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623359
• MyVariant Identifiers: chr13:g.28592657A>T (hg19) ; chr13:g.28018520A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018520A>T , CM000675.2:g.28018520A>T	GRCh38
NC_000013.10:g.28592657A>T , CM000675.1:g.28592657A>T	GRCh37
NC_000013.9:g.27490657A>T	NCBI36
NG_007066.1:g.87049T>A , LRG_457:g.87049T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2488T>A MANE Select	ENSP00000241453.7:p.Phe830Ile
ENST00000241453.11:c.2488T>A	ENSP00000241453.7:p.Phe830Ile
ENST00000380987.2:c.*400T>A	ENSP00000370374.2:n.*400T>A
NM_004119.2:c.2488T>A , LRG_457t1:c.2488T>A	NP_004110.2:p.Phe830Ile
NR_130706.1:n.2702T>A
XM_011535015.1:c.2431T>A	XP_011533317.1:p.Phe811Ile
XM_011535016.1:c.1963T>A	XP_011533318.1:p.Phe655Ile
XM_011535017.1:c.1963T>A	XP_011533319.1:p.Phe655Ile
XM_011535018.1:c.1963T>A	XP_011533320.1:p.Phe655Ile
XM_011535015.2:c.2431T>A	XP_011533317.1:p.Phe811Ile
XM_011535017.2:c.1963T>A	XP_011533319.1:p.Phe655Ile
XM_011535018.2:c.1963T>A	XP_011533320.1:p.Phe655Ile
XM_017020486.1:c.2272T>A	XP_016875975.1:p.Phe758Ile
XM_017020487.1:c.1963T>A	XP_016875976.1:p.Phe655Ile
XM_017020488.1:c.1609T>A	XP_016875977.1:p.Phe537Ile
XM_017020489.1:c.1591T>A	XP_016875978.1:p.Phe531Ile
NM_004119.3:c.2488T>A MANE Select	NP_004110.2:p.Phe830Ile
NR_130706.2:n.2686T>A