Canonical Allele Identifier: CA387650364

Gene: FLT3

Linked Data

• dbSNP Id: rs2137624230
• MyVariant Identifiers: chr13:g.28592719T>C (hg19) ; chr13:g.28018582T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018582T>C , CM000675.2:g.28018582T>C	GRCh38
NC_000013.10:g.28592719T>C , CM000675.1:g.28592719T>C	GRCh37
NC_000013.9:g.27490719T>C	NCBI36
NG_007066.1:g.86987A>G , LRG_457:g.86987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2426A>G MANE Select	ENSP00000241453.7:p.His809Arg
ENST00000241453.11:c.2426A>G	ENSP00000241453.7:p.His809Arg
ENST00000380987.2:c.*338A>G	ENSP00000370374.2:n.*338A>G
NM_004119.2:c.2426A>G , LRG_457t1:c.2426A>G	NP_004110.2:p.His809Arg
NR_130706.1:n.2640A>G
XM_011535015.1:c.2369A>G	XP_011533317.1:p.His790Arg
XM_011535016.1:c.1901A>G	XP_011533318.1:p.His634Arg
XM_011535017.1:c.1901A>G	XP_011533319.1:p.His634Arg
XM_011535018.1:c.1901A>G	XP_011533320.1:p.His634Arg
XM_011535015.2:c.2369A>G	XP_011533317.1:p.His790Arg
XM_011535017.2:c.1901A>G	XP_011533319.1:p.His634Arg
XM_011535018.2:c.1901A>G	XP_011533320.1:p.His634Arg
XM_017020486.1:c.2210A>G	XP_016875975.1:p.His737Arg
XM_017020487.1:c.1901A>G	XP_016875976.1:p.His634Arg
XM_017020488.1:c.1547A>G	XP_016875977.1:p.His516Arg
XM_017020489.1:c.1529A>G	XP_016875978.1:p.His510Arg
NM_004119.3:c.2426A>G MANE Select	NP_004110.2:p.His809Arg
NR_130706.2:n.2624A>G