Canonical Allele Identifier: CA2080781874

Gene: FLT3

Linked Data

• dbSNP Id: rs1872125819

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018860_28018861del , CM000675.2:g.28018860_28018861del	GRCh38
NC_000013.10:g.28592997_28592998del , CM000675.1:g.28592997_28592998del	GRCh37
NC_000013.9:g.27490997_27490998del	NCBI36
NG_007066.1:g.86708_86709del , LRG_457:g.86708_86709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-272_2419-271del MANE Select	ENSP00000241453.7:n.2419-272_2419-271del
ENST00000241453.11:c.2419-272_2419-271del	ENSP00000241453.7:n.2419-272_2419-271del
ENST00000380987.2:c.*331-272_*331-271del	ENSP00000370374.2:n.*331-272_*331-271del
NM_004119.2:c.2419-272_2419-271del , LRG_457t1:c.2419-272_2419-271del	NP_004110.2:n.2419-272_2419-271del
NR_130706.1:n.2633-272_2633-271del
XM_011535015.1:c.2362-272_2362-271del	XP_011533317.1:n.2362-272_2362-271del
XM_011535016.1:c.1894-272_1894-271del	XP_011533318.1:n.1894-272_1894-271del
XM_011535017.1:c.1894-272_1894-271del	XP_011533319.1:n.1894-272_1894-271del
XM_011535018.1:c.1894-272_1894-271del	XP_011533320.1:n.1894-272_1894-271del
XM_011535015.2:c.2362-272_2362-271del	XP_011533317.1:n.2362-272_2362-271del
XM_011535017.2:c.1894-272_1894-271del	XP_011533319.1:n.1894-272_1894-271del
XM_011535018.2:c.1894-272_1894-271del	XP_011533320.1:n.1894-272_1894-271del
XM_017020486.1:c.2203-272_2203-271del	XP_016875975.1:n.2203-272_2203-271del
XM_017020487.1:c.1894-272_1894-271del	XP_016875976.1:n.1894-272_1894-271del
XM_017020488.1:c.1540-272_1540-271del	XP_016875977.1:n.1540-272_1540-271del
XM_017020489.1:c.1522-272_1522-271del	XP_016875978.1:n.1522-272_1522-271del
NM_004119.3:c.2419-272_2419-271del MANE Select	NP_004110.2:n.2419-272_2419-271del
NR_130706.2:n.2617-272_2617-271del