Canonical Allele Identifier: CA387652298

Gene: FLT3

Linked Data

• dbSNP Id: rs1057519768
• MyVariant Identifiers: chr13:g.28602416T>G (hg19) ; chr13:g.28028279T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028279T>G , CM000675.2:g.28028279T>G	GRCh38
NC_000013.10:g.28602416T>G , CM000675.1:g.28602416T>G	GRCh37
NC_000013.9:g.27500416T>G	NCBI36
NG_007066.1:g.77290A>C , LRG_457:g.77290A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.1952A>C MANE Select	ENSP00000241453.7:p.Asp651Ala
ENST00000241453.11:c.1952A>C	ENSP00000241453.7:p.Asp651Ala
ENST00000380987.2:c.1952A>C	ENSP00000370374.2:p.Asp651Ala
NM_004119.2:c.1952A>C , LRG_457t1:c.1952A>C	NP_004110.2:p.Asp651Ala
NR_130706.1:n.2034A>C
XM_011535015.1:c.1895A>C	XP_011533317.1:p.Asp632Ala
XM_011535016.1:c.1427A>C	XP_011533318.1:p.Asp476Ala
XM_011535017.1:c.1427A>C	XP_011533319.1:p.Asp476Ala
XM_011535018.1:c.1427A>C	XP_011533320.1:p.Asp476Ala
XM_011535015.2:c.1895A>C	XP_011533317.1:p.Asp632Ala
XM_011535017.2:c.1427A>C	XP_011533319.1:p.Asp476Ala
XM_011535018.2:c.1427A>C	XP_011533320.1:p.Asp476Ala
XM_017020486.1:c.1736A>C	XP_016875975.1:p.Asp579Ala
XM_017020487.1:c.1427A>C	XP_016875976.1:p.Asp476Ala
XM_017020488.1:c.1073A>C	XP_016875977.1:p.Asp358Ala
XM_017020489.1:c.1055A>C	XP_016875978.1:p.Asp352Ala
NM_004119.3:c.1952A>C MANE Select	NP_004110.2:p.Asp651Ala
NR_130706.2:n.2018A>C