Canonical Allele Identifier: CA483042282

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28592703G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018566G>T , CM000675.2:g.28018566G>T	GRCh38
NC_000013.10:g.28592703G>T , CM000675.1:g.28592703G>T	GRCh37
NC_000013.9:g.27490703G>T	NCBI36
NG_007066.1:g.87003C>A , LRG_457:g.87003C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2442C>A MANE Select	ENSP00000241453.7:p.Ala814=
ENST00000241453.11:c.2442C>A	ENSP00000241453.7:p.Ala814=
ENST00000380987.2:c.*354C>A	ENSP00000370374.2:n.*354C>A
NM_004119.2:c.2442C>A , LRG_457t1:c.2442C>A	NP_004110.2:p.Ala814=
NR_130706.1:n.2656C>A
XM_011535015.1:c.2385C>A	XP_011533317.1:p.Ala795=
XM_011535016.1:c.1917C>A	XP_011533318.1:p.Ala639=
XM_011535017.1:c.1917C>A	XP_011533319.1:p.Ala639=
XM_011535018.1:c.1917C>A	XP_011533320.1:p.Ala639=
XM_011535015.2:c.2385C>A	XP_011533317.1:p.Ala795=
XM_011535017.2:c.1917C>A	XP_011533319.1:p.Ala639=
XM_011535018.2:c.1917C>A	XP_011533320.1:p.Ala639=
XM_017020486.1:c.2226C>A	XP_016875975.1:p.Ala742=
XM_017020487.1:c.1917C>A	XP_016875976.1:p.Ala639=
XM_017020488.1:c.1563C>A	XP_016875977.1:p.Ala521=
XM_017020489.1:c.1545C>A	XP_016875978.1:p.Ala515=
NM_004119.3:c.2442C>A MANE Select	NP_004110.2:p.Ala814=
NR_130706.2:n.2640C>A