Canonical Allele Identifier: CA6928568

Gene: FLT3

Linked Data

• dbSNP Id: rs747607608
• ExAC: 13:28608347 A / C
• gnomAD v2: 13-28608347-A-C
• MyVariant Identifiers: chr13:g.28608347A>C (hg19) ; chr13:g.28034210A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034210A>C , CM000675.2:g.28034210A>C	GRCh38
NC_000013.10:g.28608347A>C , CM000675.1:g.28608347A>C	GRCh37
NC_000013.9:g.27506347A>C	NCBI36
NG_007066.1:g.71359T>G , LRG_457:g.71359T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1709T>G MANE Select	ENSP00000241453.7:p.Phe570Cys
ENST00000241453.11:c.1709T>G	ENSP00000241453.7:p.Phe570Cys
ENST00000380987.2:c.1709T>G	ENSP00000370374.2:p.Phe570Cys
NM_004119.2:c.1709T>G , LRG_457t1:c.1709T>G	NP_004110.2:p.Phe570Cys
NR_130706.1:n.1791T>G
XM_011535015.1:c.1652T>G	XP_011533317.1:p.Phe551Cys
XM_011535016.1:c.1184T>G	XP_011533318.1:p.Phe395Cys
XM_011535017.1:c.1184T>G	XP_011533319.1:p.Phe395Cys
XM_011535018.1:c.1184T>G	XP_011533320.1:p.Phe395Cys
XM_011535015.2:c.1652T>G	XP_011533317.1:p.Phe551Cys
XM_011535017.2:c.1184T>G	XP_011533319.1:p.Phe395Cys
XM_011535018.2:c.1184T>G	XP_011533320.1:p.Phe395Cys
XM_017020486.1:c.1493T>G	XP_016875975.1:p.Phe498Cys
XM_017020487.1:c.1184T>G	XP_016875976.1:p.Phe395Cys
XM_017020488.1:c.830T>G	XP_016875977.1:p.Phe277Cys
XM_017020489.1:c.812T>G	XP_016875978.1:p.Phe271Cys
NM_004119.3:c.1709T>G MANE Select	NP_004110.2:p.Phe570Cys
NR_130706.2:n.1775T>G