Canonical Allele Identifier: CA387652256

Gene: FLT3

Linked Data

• dbSNP Id: rs2137655804
• MyVariant Identifiers: chr13:g.28602398G>A (hg19) ; chr13:g.28028261G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028261G>A , CM000675.2:g.28028261G>A	GRCh38
NC_000013.10:g.28602398G>A , CM000675.1:g.28602398G>A	GRCh37
NC_000013.9:g.27500398G>A	NCBI36
NG_007066.1:g.77308C>T , LRG_457:g.77308C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1970C>T MANE Select	ENSP00000241453.7:p.Ala657Val
ENST00000241453.11:c.1970C>T	ENSP00000241453.7:p.Ala657Val
ENST00000380987.2:c.1970C>T	ENSP00000370374.2:p.Ala657Val
NM_004119.2:c.1970C>T , LRG_457t1:c.1970C>T	NP_004110.2:p.Ala657Val
NR_130706.1:n.2052C>T
XM_011535015.1:c.1913C>T	XP_011533317.1:p.Ala638Val
XM_011535016.1:c.1445C>T	XP_011533318.1:p.Ala482Val
XM_011535017.1:c.1445C>T	XP_011533319.1:p.Ala482Val
XM_011535018.1:c.1445C>T	XP_011533320.1:p.Ala482Val
XM_011535015.2:c.1913C>T	XP_011533317.1:p.Ala638Val
XM_011535017.2:c.1445C>T	XP_011533319.1:p.Ala482Val
XM_011535018.2:c.1445C>T	XP_011533320.1:p.Ala482Val
XM_017020486.1:c.1754C>T	XP_016875975.1:p.Ala585Val
XM_017020487.1:c.1445C>T	XP_016875976.1:p.Ala482Val
XM_017020488.1:c.1091C>T	XP_016875977.1:p.Ala364Val
XM_017020489.1:c.1073C>T	XP_016875978.1:p.Ala358Val
NM_004119.3:c.1970C>T MANE Select	NP_004110.2:p.Ala657Val
NR_130706.2:n.2036C>T