Canonical Allele Identifier: CA2622472741
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28028104_28028106del , CM000675.2:g.28028104_28028106del GRCh38
NC_000013.10:g.28602241_28602243del , CM000675.1:g.28602241_28602243del GRCh37
NC_000013.9:g.27500241_27500243del NCBI36
NG_007066.1:g.77463_77465del , LRG_457:g.77463_77465del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2053+72_2053+74del MANE Select ENSP00000241453.7:n.2053+72_2053+74del
ENST00000241453.11:c.2053+72_2053+74del ENSP00000241453.7:n.2053+72_2053+74del
ENST00000380987.2:c.2053+72_2053+74del ENSP00000370374.2:n.2053+72_2053+74del
NM_004119.2:c.2053+72_2053+74del , LRG_457t1:c.2053+72_2053+74del NP_004110.2:n.2053+72_2053+74del
NR_130706.1:n.2135+72_2135+74del
XM_011535015.1:c.1996+72_1996+74del XP_011533317.1:n.1996+72_1996+74del
XM_011535016.1:c.1528+72_1528+74del XP_011533318.1:n.1528+72_1528+74del
XM_011535017.1:c.1528+72_1528+74del XP_011533319.1:n.1528+72_1528+74del
XM_011535018.1:c.1528+72_1528+74del XP_011533320.1:n.1528+72_1528+74del
XM_011535015.2:c.1996+72_1996+74del XP_011533317.1:n.1996+72_1996+74del
XM_011535017.2:c.1528+72_1528+74del XP_011533319.1:n.1528+72_1528+74del
XM_011535018.2:c.1528+72_1528+74del XP_011533320.1:n.1528+72_1528+74del
XM_017020486.1:c.1837+72_1837+74del XP_016875975.1:n.1837+72_1837+74del
XM_017020487.1:c.1528+72_1528+74del XP_016875976.1:n.1528+72_1528+74del
XM_017020488.1:c.1174+72_1174+74del XP_016875977.1:n.1174+72_1174+74del
XM_017020489.1:c.1156+72_1156+74del XP_016875978.1:n.1156+72_1156+74del
NM_004119.3:c.2053+72_2053+74del MANE Select NP_004110.2:n.2053+72_2053+74del
NR_130706.2:n.2119+72_2119+74del