Canonical Allele Identifier: CA2018007642
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034079_28034138dup , CM000675.2:g.28034079_28034138dup GRCh38
NC_000013.10:g.28608216_28608275dup , CM000675.1:g.28608216_28608275dup GRCh37
NC_000013.9:g.27506216_27506275dup NCBI36
NG_007066.1:g.71431_71490dup , LRG_457:g.71431_71490dup

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.1781_1837+3dup
ENST00000241453.11:c.1781_1837+3dup
ENST00000380987.2:c.1781_1837+3dup
NM_004119.2:c.1781_1837+3dup , LRG_457t1:c.1781_1837+3dup
NR_130706.1:n.1863_1919+3dup
XM_011535015.1:c.1724_1780+3dup
XM_011535016.1:c.1256_1312+3dup
XM_011535017.1:c.1256_1312+3dup
XM_011535018.1:c.1256_1312+3dup
XM_011535015.2:c.1724_1780+3dup
XM_011535017.2:c.1256_1312+3dup
XM_011535018.2:c.1256_1312+3dup
XM_017020486.1:c.1565_1621+3dup
XM_017020487.1:c.1256_1312+3dup
XM_017020488.1:c.902_958+3dup
XM_017020489.1:c.884_940+3dup
NM_004119.3:c.1781_1837+3dup
NR_130706.2:n.1847_1903+3dup