Canonical Allele Identifier: CA387652305

Gene: FLT3

Linked Data

• dbSNP Id: rs1271652776
• gnomAD v4: 13-28028282-G-T
• MyVariant Identifiers: chr13:g.28602419G>T (hg19) ; chr13:g.28028282G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028282G>T , CM000675.2:g.28028282G>T	GRCh38
NC_000013.10:g.28602419G>T , CM000675.1:g.28602419G>T	GRCh37
NC_000013.9:g.27500419G>T	NCBI36
NG_007066.1:g.77287C>A , LRG_457:g.77287C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1949C>A MANE Select	ENSP00000241453.7:p.Ala650Glu
ENST00000241453.11:c.1949C>A	ENSP00000241453.7:p.Ala650Glu
ENST00000380987.2:c.1949C>A	ENSP00000370374.2:p.Ala650Glu
NM_004119.2:c.1949C>A , LRG_457t1:c.1949C>A	NP_004110.2:p.Ala650Glu
NR_130706.1:n.2031C>A
XM_011535015.1:c.1892C>A	XP_011533317.1:p.Ala631Glu
XM_011535016.1:c.1424C>A	XP_011533318.1:p.Ala475Glu
XM_011535017.1:c.1424C>A	XP_011533319.1:p.Ala475Glu
XM_011535018.1:c.1424C>A	XP_011533320.1:p.Ala475Glu
XM_011535015.2:c.1892C>A	XP_011533317.1:p.Ala631Glu
XM_011535017.2:c.1424C>A	XP_011533319.1:p.Ala475Glu
XM_011535018.2:c.1424C>A	XP_011533320.1:p.Ala475Glu
XM_017020486.1:c.1733C>A	XP_016875975.1:p.Ala578Glu
XM_017020487.1:c.1424C>A	XP_016875976.1:p.Ala475Glu
XM_017020488.1:c.1070C>A	XP_016875977.1:p.Ala357Glu
XM_017020489.1:c.1052C>A	XP_016875978.1:p.Ala351Glu
NM_004119.3:c.1949C>A MANE Select	NP_004110.2:p.Ala650Glu
NR_130706.2:n.2015C>A