Canonical Allele Identifier: CA387640973

Gene: FLT3

Linked Data

• dbSNP Id: rs779699008
• MyVariant Identifiers: chr13:g.28608315C>A (hg19) ; chr13:g.28034178C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034178C>A , CM000675.2:g.28034178C>A	GRCh38
NC_000013.10:g.28608315C>A , CM000675.1:g.28608315C>A	GRCh37
NC_000013.9:g.27506315C>A	NCBI36
NG_007066.1:g.71391G>T , LRG_457:g.71391G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1741G>T MANE Select	ENSP00000241453.7:p.Val581Leu
ENST00000241453.11:c.1741G>T	ENSP00000241453.7:p.Val581Leu
ENST00000380987.2:c.1741G>T	ENSP00000370374.2:p.Val581Leu
NM_004119.2:c.1741G>T , LRG_457t1:c.1741G>T	NP_004110.2:p.Val581Leu
NR_130706.1:n.1823G>T
XM_011535015.1:c.1684G>T	XP_011533317.1:p.Val562Leu
XM_011535016.1:c.1216G>T	XP_011533318.1:p.Val406Leu
XM_011535017.1:c.1216G>T	XP_011533319.1:p.Val406Leu
XM_011535018.1:c.1216G>T	XP_011533320.1:p.Val406Leu
XM_011535015.2:c.1684G>T	XP_011533317.1:p.Val562Leu
XM_011535017.2:c.1216G>T	XP_011533319.1:p.Val406Leu
XM_011535018.2:c.1216G>T	XP_011533320.1:p.Val406Leu
XM_017020486.1:c.1525G>T	XP_016875975.1:p.Val509Leu
XM_017020487.1:c.1216G>T	XP_016875976.1:p.Val406Leu
XM_017020488.1:c.862G>T	XP_016875977.1:p.Val288Leu
XM_017020489.1:c.844G>T	XP_016875978.1:p.Val282Leu
NM_004119.3:c.1741G>T MANE Select	NP_004110.2:p.Val581Leu
NR_130706.2:n.1807G>T