Canonical Allele Identifier: CA645598057
Gene: FLT3 HGNC NCBI

Linked Data

COSMIC: COSM19852

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28034185_28034186delinsTGGTGGGTTCCTTAAGT , CM000675.2:g.28034185_28034186delinsTGGTGGGTTCCTTAAGT GRCh38
NC_000013.10:g.28608322_28608323delinsTGGTGGGTTCCTTAAGT , CM000675.1:g.28608322_28608323delinsTGGTGGGTTCCTTAAGT GRCh37
NC_000013.9:g.27506322_27506323delinsTGGTGGGTTCCTTAAGT NCBI36
NG_007066.1:g.71383_71384delinsACTTAAGGAACCCACCA , LRG_457:g.71383_71384delinsACTTAAGGAACCCACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.1733_1734delinsACTTAAGGAACCCACCA MANE Select ENSP00000241453.7:p.Met578delinsAsnLeuArgAsnProPro
ENST00000241453.11:c.1733_1734delinsACTTAAGGAACCCACCA ENSP00000241453.7:p.Met578delinsAsnLeuArgAsnProPro
ENST00000380987.2:c.1733_1734delinsACTTAAGGAACCCACCA ENSP00000370374.2:p.Met578delinsAsnLeuArgAsnProPro
NM_004119.2:c.1733_1734delinsACTTAAGGAACCCACCA , LRG_457t1:c.1733_1734delinsACTTAAGGAACCCACCA NP_004110.2:p.Met578delinsAsnLeuArgAsnProPro
NR_130706.1:n.1815_1816delinsACTTAAGGAACCCACCA
XM_011535015.1:c.1676_1677delinsACTTAAGGAACCCACCA XP_011533317.1:p.Met559delinsAsnLeuArgAsnProPro
XM_011535016.1:c.1208_1209delinsACTTAAGGAACCCACCA XP_011533318.1:p.Met403delinsAsnLeuArgAsnProPro
XM_011535017.1:c.1208_1209delinsACTTAAGGAACCCACCA XP_011533319.1:p.Met403delinsAsnLeuArgAsnProPro
XM_011535018.1:c.1208_1209delinsACTTAAGGAACCCACCA XP_011533320.1:p.Met403delinsAsnLeuArgAsnProPro
XM_011535015.2:c.1676_1677delinsACTTAAGGAACCCACCA XP_011533317.1:p.Met559delinsAsnLeuArgAsnProPro
XM_011535017.2:c.1208_1209delinsACTTAAGGAACCCACCA XP_011533319.1:p.Met403delinsAsnLeuArgAsnProPro
XM_011535018.2:c.1208_1209delinsACTTAAGGAACCCACCA XP_011533320.1:p.Met403delinsAsnLeuArgAsnProPro
XM_017020486.1:c.1517_1518delinsACTTAAGGAACCCACCA XP_016875975.1:p.Met506delinsAsnLeuArgAsnProPro
XM_017020487.1:c.1208_1209delinsACTTAAGGAACCCACCA XP_016875976.1:p.Met403delinsAsnLeuArgAsnProPro
XM_017020488.1:c.854_855delinsACTTAAGGAACCCACCA XP_016875977.1:p.Met285delinsAsnLeuArgAsnProPro
XM_017020489.1:c.836_837delinsACTTAAGGAACCCACCA XP_016875978.1:p.Met279delinsAsnLeuArgAsnProPro
NM_004119.3:c.1733_1734delinsACTTAAGGAACCCACCA MANE Select NP_004110.2:p.Met578delinsAsnLeuArgAsnProPro
NR_130706.2:n.1799_1800delinsACTTAAGGAACCCACCA