Canonical Allele Identifier: CA387650256

Gene: FLT3

Linked Data

• dbSNP Id: rs1403972292
• gnomAD v2: 13-28592668-T-C
• gnomAD v4: 13-28018531-T-C
• MyVariant Identifiers: chr13:g.28592668T>C (hg19) ; chr13:g.28018531T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018531T>C , CM000675.2:g.28018531T>C	GRCh38
NC_000013.10:g.28592668T>C , CM000675.1:g.28592668T>C	GRCh37
NC_000013.9:g.27490668T>C	NCBI36
NG_007066.1:g.87038A>G , LRG_457:g.87038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2477A>G MANE Select	ENSP00000241453.7:p.Lys826Arg
ENST00000241453.11:c.2477A>G	ENSP00000241453.7:p.Lys826Arg
ENST00000380987.2:c.*389A>G	ENSP00000370374.2:n.*389A>G
NM_004119.2:c.2477A>G , LRG_457t1:c.2477A>G	NP_004110.2:p.Lys826Arg
NR_130706.1:n.2691A>G
XM_011535015.1:c.2420A>G	XP_011533317.1:p.Lys807Arg
XM_011535016.1:c.1952A>G	XP_011533318.1:p.Lys651Arg
XM_011535017.1:c.1952A>G	XP_011533319.1:p.Lys651Arg
XM_011535018.1:c.1952A>G	XP_011533320.1:p.Lys651Arg
XM_011535015.2:c.2420A>G	XP_011533317.1:p.Lys807Arg
XM_011535017.2:c.1952A>G	XP_011533319.1:p.Lys651Arg
XM_011535018.2:c.1952A>G	XP_011533320.1:p.Lys651Arg
XM_017020486.1:c.2261A>G	XP_016875975.1:p.Lys754Arg
XM_017020487.1:c.1952A>G	XP_016875976.1:p.Lys651Arg
XM_017020488.1:c.1598A>G	XP_016875977.1:p.Lys533Arg
XM_017020489.1:c.1580A>G	XP_016875978.1:p.Lys527Arg
NM_004119.3:c.2477A>G MANE Select	NP_004110.2:p.Lys826Arg
NR_130706.2:n.2675A>G