Canonical Allele Identifier: CA387652283

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28602408C>T (hg19) ; chr13:g.28028271C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028271C>T , CM000675.2:g.28028271C>T	GRCh38
NC_000013.10:g.28602408C>T , CM000675.1:g.28602408C>T	GRCh37
NC_000013.9:g.27500408C>T	NCBI36
NG_007066.1:g.77298G>A , LRG_457:g.77298G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1960G>A MANE Select	ENSP00000241453.7:p.Glu654Lys
ENST00000241453.11:c.1960G>A	ENSP00000241453.7:p.Glu654Lys
ENST00000380987.2:c.1960G>A	ENSP00000370374.2:p.Glu654Lys
NM_004119.2:c.1960G>A , LRG_457t1:c.1960G>A	NP_004110.2:p.Glu654Lys
NR_130706.1:n.2042G>A
XM_011535015.1:c.1903G>A	XP_011533317.1:p.Glu635Lys
XM_011535016.1:c.1435G>A	XP_011533318.1:p.Glu479Lys
XM_011535017.1:c.1435G>A	XP_011533319.1:p.Glu479Lys
XM_011535018.1:c.1435G>A	XP_011533320.1:p.Glu479Lys
XM_011535015.2:c.1903G>A	XP_011533317.1:p.Glu635Lys
XM_011535017.2:c.1435G>A	XP_011533319.1:p.Glu479Lys
XM_011535018.2:c.1435G>A	XP_011533320.1:p.Glu479Lys
XM_017020486.1:c.1744G>A	XP_016875975.1:p.Glu582Lys
XM_017020487.1:c.1435G>A	XP_016875976.1:p.Glu479Lys
XM_017020488.1:c.1081G>A	XP_016875977.1:p.Glu361Lys
XM_017020489.1:c.1063G>A	XP_016875978.1:p.Glu355Lys
NM_004119.3:c.1960G>A MANE Select	NP_004110.2:p.Glu654Lys
NR_130706.2:n.2026G>A