Canonical Allele Identifier: CA387650383

Gene: FLT3

Linked Data

• dbSNP Id: rs751383392
• MyVariant Identifiers: chr13:g.28592724A>T (hg19) ; chr13:g.28018587A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018587A>T , CM000675.2:g.28018587A>T	GRCh38
NC_000013.10:g.28592724A>T , CM000675.1:g.28592724A>T	GRCh37
NC_000013.9:g.27490724A>T	NCBI36
NG_007066.1:g.86982T>A , LRG_457:g.86982T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2421T>A MANE Select	ENSP00000241453.7:p.Cys807Ter
ENST00000241453.11:c.2421T>A	ENSP00000241453.7:p.Cys807Ter
ENST00000380987.2:c.*333T>A	ENSP00000370374.2:n.*333T>A
NM_004119.2:c.2421T>A , LRG_457t1:c.2421T>A	NP_004110.2:p.Cys807Ter
NR_130706.1:n.2635T>A
XM_011535015.1:c.2364T>A	XP_011533317.1:p.Cys788Ter
XM_011535016.1:c.1896T>A	XP_011533318.1:p.Cys632Ter
XM_011535017.1:c.1896T>A	XP_011533319.1:p.Cys632Ter
XM_011535018.1:c.1896T>A	XP_011533320.1:p.Cys632Ter
XM_011535015.2:c.2364T>A	XP_011533317.1:p.Cys788Ter
XM_011535017.2:c.1896T>A	XP_011533319.1:p.Cys632Ter
XM_011535018.2:c.1896T>A	XP_011533320.1:p.Cys632Ter
XM_017020486.1:c.2205T>A	XP_016875975.1:p.Cys735Ter
XM_017020487.1:c.1896T>A	XP_016875976.1:p.Cys632Ter
XM_017020488.1:c.1542T>A	XP_016875977.1:p.Cys514Ter
XM_017020489.1:c.1524T>A	XP_016875978.1:p.Cys508Ter
NM_004119.3:c.2421T>A MANE Select	NP_004110.2:p.Cys807Ter
NR_130706.2:n.2619T>A