Canonical Allele Identifier: CA645597739

Gene: FLT3

Linked Data

• COSMIC: COSM5879411

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034081_28034116dup , CM000675.2:g.28034081_28034116dup	GRCh38
NC_000013.10:g.28608218_28608253dup , CM000675.1:g.28608218_28608253dup	GRCh37
NC_000013.9:g.27506218_27506253dup	NCBI36
NG_007066.1:g.71453_71488dup , LRG_457:g.71453_71488dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1803_1837+1dup
ENST00000241453.11:c.1803_1837+1dup
ENST00000380987.2:c.1803_1837+1dup
NM_004119.2:c.1803_1837+1dup , LRG_457t1:c.1803_1837+1dup
NR_130706.1:n.1885_1919+1dup
XM_011535015.1:c.1746_1780+1dup
XM_011535016.1:c.1278_1312+1dup
XM_011535017.1:c.1278_1312+1dup
XM_011535018.1:c.1278_1312+1dup
XM_011535015.2:c.1746_1780+1dup
XM_011535017.2:c.1278_1312+1dup
XM_011535018.2:c.1278_1312+1dup
XM_017020486.1:c.1587_1621+1dup
XM_017020487.1:c.1278_1312+1dup
XM_017020488.1:c.924_958+1dup
XM_017020489.1:c.906_940+1dup
NM_004119.3:c.1803_1837+1dup
NR_130706.2:n.1869_1903+1dup