Canonical Allele Identifier: CA645597728
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034078_28034164dup , CM000675.2:g.28034078_28034164dup GRCh38
NC_000013.10:g.28608215_28608301dup , CM000675.1:g.28608215_28608301dup GRCh37
NC_000013.9:g.27506215_27506301dup NCBI36
NG_007066.1:g.71405_71491dup , LRG_457:g.71405_71491dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1755_1837+4dup
ENST00000241453.11:c.1755_1837+4dup
ENST00000380987.2:c.1755_1837+4dup
NM_004119.2:c.1755_1837+4dup , LRG_457t1:c.1755_1837+4dup
NR_130706.1:n.1837_1919+4dup
XM_011535015.1:c.1698_1780+4dup
XM_011535016.1:c.1230_1312+4dup
XM_011535017.1:c.1230_1312+4dup
XM_011535018.1:c.1230_1312+4dup
XM_011535015.2:c.1698_1780+4dup
XM_011535017.2:c.1230_1312+4dup
XM_011535018.2:c.1230_1312+4dup
XM_017020486.1:c.1539_1621+4dup
XM_017020487.1:c.1230_1312+4dup
XM_017020488.1:c.876_958+4dup
XM_017020489.1:c.858_940+4dup
NM_004119.3:c.1755_1837+4dup
NR_130706.2:n.1821_1903+4dup