Canonical Allele Identifier: CA645597694
Gene: FLT3 HGNC NCBI

Linked Data

COSMIC: COSM19435

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018501_28018502delinsTCCAA , CM000675.2:g.28018501_28018502delinsTCCAA GRCh38
NC_000013.10:g.28592638_28592639delinsTCCAA , CM000675.1:g.28592638_28592639delinsTCCAA GRCh37
NC_000013.9:g.27490638_27490639delinsTCCAA NCBI36
NG_007066.1:g.87067_87068delinsTTGGA , LRG_457:g.87067_87068delinsTTGGA

Transcript Alleles

HGVS Amino-acid change
ENST00000241453.12:c.2506_2507delinsTTGGA MANE Select ENSP00000241453.7:p.Ile836delinsLeuAsp
ENST00000241453.11:c.2506_2507delinsTTGGA ENSP00000241453.7:p.Ile836delinsLeuAsp
ENST00000380987.2:c.*418_*419delinsTTGGA ENSP00000370374.2:n.*418_*419delinsTTGGA
NM_004119.2:c.2506_2507delinsTTGGA , LRG_457t1:c.2506_2507delinsTTGGA NP_004110.2:p.Ile836delinsLeuAsp
NR_130706.1:n.2720_2721delinsTTGGA
XM_011535015.1:c.2449_2450delinsTTGGA XP_011533317.1:p.Ile817delinsLeuAsp
XM_011535016.1:c.1981_1982delinsTTGGA XP_011533318.1:p.Ile661delinsLeuAsp
XM_011535017.1:c.1981_1982delinsTTGGA XP_011533319.1:p.Ile661delinsLeuAsp
XM_011535018.1:c.1981_1982delinsTTGGA XP_011533320.1:p.Ile661delinsLeuAsp
XM_011535015.2:c.2449_2450delinsTTGGA XP_011533317.1:p.Ile817delinsLeuAsp
XM_011535017.2:c.1981_1982delinsTTGGA XP_011533319.1:p.Ile661delinsLeuAsp
XM_011535018.2:c.1981_1982delinsTTGGA XP_011533320.1:p.Ile661delinsLeuAsp
XM_017020486.1:c.2290_2291delinsTTGGA XP_016875975.1:p.Ile764delinsLeuAsp
XM_017020487.1:c.1981_1982delinsTTGGA XP_016875976.1:p.Ile661delinsLeuAsp
XM_017020488.1:c.1627_1628delinsTTGGA XP_016875977.1:p.Ile543delinsLeuAsp
XM_017020489.1:c.1609_1610delinsTTGGA XP_016875978.1:p.Ile537delinsLeuAsp
NM_004119.3:c.2506_2507delinsTTGGA MANE Select NP_004110.2:p.Ile836delinsLeuAsp
NR_130706.2:n.2704_2705delinsTTGGA