Canonical Allele Identifier: CA387650342

Gene: FLT3

Linked Data

• dbSNP Id: rs1330989461
• MyVariant Identifiers: chr13:g.28592711G>T (hg19) ; chr13:g.28018574G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018574G>T , CM000675.2:g.28018574G>T	GRCh38
NC_000013.10:g.28592711G>T , CM000675.1:g.28592711G>T	GRCh37
NC_000013.9:g.27490711G>T	NCBI36
NG_007066.1:g.86995C>A , LRG_457:g.86995C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2434C>A MANE Select	ENSP00000241453.7:p.Leu812Met
ENST00000241453.11:c.2434C>A	ENSP00000241453.7:p.Leu812Met
ENST00000380987.2:c.*346C>A	ENSP00000370374.2:n.*346C>A
NM_004119.2:c.2434C>A , LRG_457t1:c.2434C>A	NP_004110.2:p.Leu812Met
NR_130706.1:n.2648C>A
XM_011535015.1:c.2377C>A	XP_011533317.1:p.Leu793Met
XM_011535016.1:c.1909C>A	XP_011533318.1:p.Leu637Met
XM_011535017.1:c.1909C>A	XP_011533319.1:p.Leu637Met
XM_011535018.1:c.1909C>A	XP_011533320.1:p.Leu637Met
XM_011535015.2:c.2377C>A	XP_011533317.1:p.Leu793Met
XM_011535017.2:c.1909C>A	XP_011533319.1:p.Leu637Met
XM_011535018.2:c.1909C>A	XP_011533320.1:p.Leu637Met
XM_017020486.1:c.2218C>A	XP_016875975.1:p.Leu740Met
XM_017020487.1:c.1909C>A	XP_016875976.1:p.Leu637Met
XM_017020488.1:c.1555C>A	XP_016875977.1:p.Leu519Met
XM_017020489.1:c.1537C>A	XP_016875978.1:p.Leu513Met
NM_004119.3:c.2434C>A MANE Select	NP_004110.2:p.Leu812Met
NR_130706.2:n.2632C>A