Canonical Allele Identifier: CA2622474435
Gene: FLT3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018359_28018360del , CM000675.2:g.28018359_28018360del GRCh38
NC_000013.10:g.28592496_28592497del , CM000675.1:g.28592496_28592497del GRCh37
NC_000013.9:g.27490496_27490497del NCBI36
NG_007066.1:g.87209_87210del , LRG_457:g.87209_87210del

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2541+107_2541+108del MANE Select ENSP00000241453.7:n.2541+107_2541+108del
ENST00000241453.11:c.2541+107_2541+108del ENSP00000241453.7:n.2541+107_2541+108del
ENST00000380987.2:c.*453+107_*453+108del ENSP00000370374.2:n.*453+107_*453+108del
NM_004119.2:c.2541+107_2541+108del , LRG_457t1:c.2541+107_2541+108del NP_004110.2:n.2541+107_2541+108del
NR_130706.1:n.2755+107_2755+108del
XM_011535015.1:c.2484+107_2484+108del XP_011533317.1:n.2484+107_2484+108del
XM_011535016.1:c.2016+107_2016+108del XP_011533318.1:n.2016+107_2016+108del
XM_011535017.1:c.2016+107_2016+108del XP_011533319.1:n.2016+107_2016+108del
XM_011535018.1:c.2016+107_2016+108del XP_011533320.1:n.2016+107_2016+108del
XM_011535015.2:c.2484+107_2484+108del XP_011533317.1:n.2484+107_2484+108del
XM_011535017.2:c.2016+107_2016+108del XP_011533319.1:n.2016+107_2016+108del
XM_011535018.2:c.2016+107_2016+108del XP_011533320.1:n.2016+107_2016+108del
XM_017020486.1:c.2325+107_2325+108del XP_016875975.1:n.2325+107_2325+108del
XM_017020487.1:c.2016+107_2016+108del XP_016875976.1:n.2016+107_2016+108del
XM_017020488.1:c.1662+107_1662+108del XP_016875977.1:n.1662+107_1662+108del
XM_017020489.1:c.1644+107_1644+108del XP_016875978.1:n.1644+107_1644+108del
NM_004119.3:c.2541+107_2541+108del MANE Select NP_004110.2:n.2541+107_2541+108del
NR_130706.2:n.2739+107_2739+108del