Canonical Allele Identifier: CA387650296

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623745
• MyVariant Identifiers: chr13:g.28592687T>G (hg19) ; chr13:g.28018550T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018550T>G , CM000675.2:g.28018550T>G	GRCh38
NC_000013.10:g.28592687T>G , CM000675.1:g.28592687T>G	GRCh37
NC_000013.9:g.27490687T>G	NCBI36
NG_007066.1:g.87019A>C , LRG_457:g.87019A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2458A>C MANE Select	ENSP00000241453.7:p.Thr820Pro
ENST00000241453.11:c.2458A>C	ENSP00000241453.7:p.Thr820Pro
ENST00000380987.2:c.*370A>C	ENSP00000370374.2:n.*370A>C
NM_004119.2:c.2458A>C , LRG_457t1:c.2458A>C	NP_004110.2:p.Thr820Pro
NR_130706.1:n.2672A>C
XM_011535015.1:c.2401A>C	XP_011533317.1:p.Thr801Pro
XM_011535016.1:c.1933A>C	XP_011533318.1:p.Thr645Pro
XM_011535017.1:c.1933A>C	XP_011533319.1:p.Thr645Pro
XM_011535018.1:c.1933A>C	XP_011533320.1:p.Thr645Pro
XM_011535015.2:c.2401A>C	XP_011533317.1:p.Thr801Pro
XM_011535017.2:c.1933A>C	XP_011533319.1:p.Thr645Pro
XM_011535018.2:c.1933A>C	XP_011533320.1:p.Thr645Pro
XM_017020486.1:c.2242A>C	XP_016875975.1:p.Thr748Pro
XM_017020487.1:c.1933A>C	XP_016875976.1:p.Thr645Pro
XM_017020488.1:c.1579A>C	XP_016875977.1:p.Thr527Pro
XM_017020489.1:c.1561A>C	XP_016875978.1:p.Thr521Pro
NM_004119.3:c.2458A>C MANE Select	NP_004110.2:p.Thr820Pro
NR_130706.2:n.2656A>C