Canonical Allele Identifier: CA645597725
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034080_28034115dup , CM000675.2:g.28034080_28034115dup GRCh38
NC_000013.10:g.28608217_28608252dup , CM000675.1:g.28608217_28608252dup GRCh37
NC_000013.9:g.27506217_27506252dup NCBI36
NG_007066.1:g.71456_71491dup , LRG_457:g.71456_71491dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1806_1837+4dup
ENST00000241453.11:c.1806_1837+4dup
ENST00000380987.2:c.1806_1837+4dup
NM_004119.2:c.1806_1837+4dup , LRG_457t1:c.1806_1837+4dup
NR_130706.1:n.1888_1919+4dup
XM_011535015.1:c.1749_1780+4dup
XM_011535016.1:c.1281_1312+4dup
XM_011535017.1:c.1281_1312+4dup
XM_011535018.1:c.1281_1312+4dup
XM_011535015.2:c.1749_1780+4dup
XM_011535017.2:c.1281_1312+4dup
XM_011535018.2:c.1281_1312+4dup
XM_017020486.1:c.1590_1621+4dup
XM_017020487.1:c.1281_1312+4dup
XM_017020488.1:c.927_958+4dup
XM_017020489.1:c.909_940+4dup
NM_004119.3:c.1806_1837+4dup
NR_130706.2:n.1872_1903+4dup