Canonical Allele Identifier: CA483042270

Gene: FLT3

Linked Data

• dbSNP Id: rs2137623762
• MyVariant Identifiers: chr13:g.28592688G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018551G>A , CM000675.2:g.28018551G>A	GRCh38
NC_000013.10:g.28592688G>A , CM000675.1:g.28592688G>A	GRCh37
NC_000013.9:g.27490688G>A	NCBI36
NG_007066.1:g.87018C>T , LRG_457:g.87018C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2457C>T MANE Select	ENSP00000241453.7:p.Val819=
ENST00000241453.11:c.2457C>T	ENSP00000241453.7:p.Val819=
ENST00000380987.2:c.*369C>T	ENSP00000370374.2:n.*369C>T
NM_004119.2:c.2457C>T , LRG_457t1:c.2457C>T	NP_004110.2:p.Val819=
NR_130706.1:n.2671C>T
XM_011535015.1:c.2400C>T	XP_011533317.1:p.Val800=
XM_011535016.1:c.1932C>T	XP_011533318.1:p.Val644=
XM_011535017.1:c.1932C>T	XP_011533319.1:p.Val644=
XM_011535018.1:c.1932C>T	XP_011533320.1:p.Val644=
XM_011535015.2:c.2400C>T	XP_011533317.1:p.Val800=
XM_011535017.2:c.1932C>T	XP_011533319.1:p.Val644=
XM_011535018.2:c.1932C>T	XP_011533320.1:p.Val644=
XM_017020486.1:c.2241C>T	XP_016875975.1:p.Val747=
XM_017020487.1:c.1932C>T	XP_016875976.1:p.Val644=
XM_017020488.1:c.1578C>T	XP_016875977.1:p.Val526=
XM_017020489.1:c.1560C>T	XP_016875978.1:p.Val520=
NM_004119.3:c.2457C>T MANE Select	NP_004110.2:p.Val819=
NR_130706.2:n.2655C>T