Canonical Allele Identifier: CA645597693
Gene: FLT3 HGNC NCBI

Linked Data

COSMIC: COSM24530

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018500_28018502delinsAAA , CM000675.2:g.28018500_28018502delinsAAA GRCh38
NC_000013.10:g.28592637_28592639delinsAAA , CM000675.1:g.28592637_28592639delinsAAA GRCh37
NC_000013.9:g.27490637_27490639delinsAAA NCBI36
NG_007066.1:g.87067_87069delinsTTT , LRG_457:g.87067_87069delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2506_2508delinsTTT MANE Select ENSP00000241453.7:p.Ile836Phe
ENST00000241453.11:c.2506_2508delinsTTT ENSP00000241453.7:p.Ile836Phe
ENST00000380987.2:c.*418_*420delinsTTT ENSP00000370374.2:n.*418_*420delinsTTT
NM_004119.2:c.2506_2508delinsTTT , LRG_457t1:c.2506_2508delinsTTT NP_004110.2:p.Ile836Phe
NR_130706.1:n.2720_2722delinsTTT
XM_011535015.1:c.2449_2451delinsTTT XP_011533317.1:p.Ile817Phe
XM_011535016.1:c.1981_1983delinsTTT XP_011533318.1:p.Ile661Phe
XM_011535017.1:c.1981_1983delinsTTT XP_011533319.1:p.Ile661Phe
XM_011535018.1:c.1981_1983delinsTTT XP_011533320.1:p.Ile661Phe
XM_011535015.2:c.2449_2451delinsTTT XP_011533317.1:p.Ile817Phe
XM_011535017.2:c.1981_1983delinsTTT XP_011533319.1:p.Ile661Phe
XM_011535018.2:c.1981_1983delinsTTT XP_011533320.1:p.Ile661Phe
XM_017020486.1:c.2290_2292delinsTTT XP_016875975.1:p.Ile764Phe
XM_017020487.1:c.1981_1983delinsTTT XP_016875976.1:p.Ile661Phe
XM_017020488.1:c.1627_1629delinsTTT XP_016875977.1:p.Ile543Phe
XM_017020489.1:c.1609_1611delinsTTT XP_016875978.1:p.Ile537Phe
NM_004119.3:c.2506_2508delinsTTT MANE Select NP_004110.2:p.Ile836Phe
NR_130706.2:n.2704_2706delinsTTT