Canonical Allele Identifier: CA387650310

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623858
• MyVariant Identifiers: chr13:g.28592695A>T (hg19) ; chr13:g.28018558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018558A>T , CM000675.2:g.28018558A>T	GRCh38
NC_000013.10:g.28592695A>T , CM000675.1:g.28592695A>T	GRCh37
NC_000013.9:g.27490695A>T	NCBI36
NG_007066.1:g.87011T>A , LRG_457:g.87011T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2450T>A MANE Select	ENSP00000241453.7:p.Val817Glu
ENST00000241453.11:c.2450T>A	ENSP00000241453.7:p.Val817Glu
ENST00000380987.2:c.*362T>A	ENSP00000370374.2:n.*362T>A
NM_004119.2:c.2450T>A , LRG_457t1:c.2450T>A	NP_004110.2:p.Val817Glu
NR_130706.1:n.2664T>A
XM_011535015.1:c.2393T>A	XP_011533317.1:p.Val798Glu
XM_011535016.1:c.1925T>A	XP_011533318.1:p.Val642Glu
XM_011535017.1:c.1925T>A	XP_011533319.1:p.Val642Glu
XM_011535018.1:c.1925T>A	XP_011533320.1:p.Val642Glu
XM_011535015.2:c.2393T>A	XP_011533317.1:p.Val798Glu
XM_011535017.2:c.1925T>A	XP_011533319.1:p.Val642Glu
XM_011535018.2:c.1925T>A	XP_011533320.1:p.Val642Glu
XM_017020486.1:c.2234T>A	XP_016875975.1:p.Val745Glu
XM_017020487.1:c.1925T>A	XP_016875976.1:p.Val642Glu
XM_017020488.1:c.1571T>A	XP_016875977.1:p.Val524Glu
XM_017020489.1:c.1553T>A	XP_016875978.1:p.Val518Glu
NM_004119.3:c.2450T>A MANE Select	NP_004110.2:p.Val817Glu
NR_130706.2:n.2648T>A