Canonical Allele Identifier: CA645597737
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034080_28034145dup , CM000675.2:g.28034080_28034145dup GRCh38
NC_000013.10:g.28608217_28608282dup , CM000675.1:g.28608217_28608282dup GRCh37
NC_000013.9:g.27506217_27506282dup NCBI36
NG_007066.1:g.71424_71489dup , LRG_457:g.71424_71489dup

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.1774_1837+2dup
ENST00000241453.11:c.1774_1837+2dup
ENST00000380987.2:c.1774_1837+2dup
NM_004119.2:c.1774_1837+2dup , LRG_457t1:c.1774_1837+2dup
NR_130706.1:n.1856_1919+2dup
XM_011535015.1:c.1717_1780+2dup
XM_011535016.1:c.1249_1312+2dup
XM_011535017.1:c.1249_1312+2dup
XM_011535018.1:c.1249_1312+2dup
XM_011535015.2:c.1717_1780+2dup
XM_011535017.2:c.1249_1312+2dup
XM_011535018.2:c.1249_1312+2dup
XM_017020486.1:c.1558_1621+2dup
XM_017020487.1:c.1249_1312+2dup
XM_017020488.1:c.895_958+2dup
XM_017020489.1:c.877_940+2dup
NM_004119.3:c.1774_1837+2dup
NR_130706.2:n.1840_1903+2dup