Canonical Allele Identifier: CA387652161

Gene: FLT3

Linked Data

• ClinVar Variation Id: 2331709
• ClinVar RCV Id: RCV002940532
• dbSNP Id: rs1367367961
• gnomAD v4: 13-28028217-C-T
• MyVariant Identifiers: chr13:g.28602354C>T (hg19) ; chr13:g.28028217C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028217C>T , CM000675.2:g.28028217C>T	GRCh38
NC_000013.10:g.28602354C>T , CM000675.1:g.28602354C>T	GRCh37
NC_000013.9:g.27500354C>T	NCBI36
NG_007066.1:g.77352G>A , LRG_457:g.77352G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2014G>A MANE Select	ENSP00000241453.7:p.Glu672Lys
ENST00000241453.11:c.2014G>A	ENSP00000241453.7:p.Glu672Lys
ENST00000380987.2:c.2014G>A	ENSP00000370374.2:p.Glu672Lys
NM_004119.2:c.2014G>A , LRG_457t1:c.2014G>A	NP_004110.2:p.Glu672Lys
NR_130706.1:n.2096G>A
XM_011535015.1:c.1957G>A	XP_011533317.1:p.Glu653Lys
XM_011535016.1:c.1489G>A	XP_011533318.1:p.Glu497Lys
XM_011535017.1:c.1489G>A	XP_011533319.1:p.Glu497Lys
XM_011535018.1:c.1489G>A	XP_011533320.1:p.Glu497Lys
XM_011535015.2:c.1957G>A	XP_011533317.1:p.Glu653Lys
XM_011535017.2:c.1489G>A	XP_011533319.1:p.Glu497Lys
XM_011535018.2:c.1489G>A	XP_011533320.1:p.Glu497Lys
XM_017020486.1:c.1798G>A	XP_016875975.1:p.Glu600Lys
XM_017020487.1:c.1489G>A	XP_016875976.1:p.Glu497Lys
XM_017020488.1:c.1135G>A	XP_016875977.1:p.Glu379Lys
XM_017020489.1:c.1117G>A	XP_016875978.1:p.Glu373Lys
NM_004119.3:c.2014G>A MANE Select	NP_004110.2:p.Glu672Lys
NR_130706.2:n.2080G>A