Canonical Allele Identifier: CA2080781804

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018768_28018769delinsTA , CM000675.2:g.28018768_28018769delinsTA	GRCh38
NC_000013.10:g.28592905_28592906delinsTA , CM000675.1:g.28592905_28592906delinsTA	GRCh37
NC_000013.9:g.27490905_27490906delinsTA	NCBI36
NG_007066.1:g.86800_86801delinsTA , LRG_457:g.86800_86801delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-180_2419-179delinsTA MANE Select	ENSP00000241453.7:n.2419-180_2419-179delinsTA
ENST00000241453.11:c.2419-180_2419-179delinsTA	ENSP00000241453.7:n.2419-180_2419-179delinsTA
ENST00000380987.2:c.*331-180_*331-179delinsTA	ENSP00000370374.2:n.*331-180_*331-179delinsTA
NM_004119.2:c.2419-180_2419-179delinsTA , LRG_457t1:c.2419-180_2419-179delinsTA	NP_004110.2:n.2419-180_2419-179delinsTA
NR_130706.1:n.2633-180_2633-179delinsTA
XM_011535015.1:c.2362-180_2362-179delinsTA	XP_011533317.1:n.2362-180_2362-179delinsTA
XM_011535016.1:c.1894-180_1894-179delinsTA	XP_011533318.1:n.1894-180_1894-179delinsTA
XM_011535017.1:c.1894-180_1894-179delinsTA	XP_011533319.1:n.1894-180_1894-179delinsTA
XM_011535018.1:c.1894-180_1894-179delinsTA	XP_011533320.1:n.1894-180_1894-179delinsTA
XM_011535015.2:c.2362-180_2362-179delinsTA	XP_011533317.1:n.2362-180_2362-179delinsTA
XM_011535017.2:c.1894-180_1894-179delinsTA	XP_011533319.1:n.1894-180_1894-179delinsTA
XM_011535018.2:c.1894-180_1894-179delinsTA	XP_011533320.1:n.1894-180_1894-179delinsTA
XM_017020486.1:c.2203-180_2203-179delinsTA	XP_016875975.1:n.2203-180_2203-179delinsTA
XM_017020487.1:c.1894-180_1894-179delinsTA	XP_016875976.1:n.1894-180_1894-179delinsTA
XM_017020488.1:c.1540-180_1540-179delinsTA	XP_016875977.1:n.1540-180_1540-179delinsTA
XM_017020489.1:c.1522-180_1522-179delinsTA	XP_016875978.1:n.1522-180_1522-179delinsTA
NM_004119.3:c.2419-180_2419-179delinsTA MANE Select	NP_004110.2:n.2419-180_2419-179delinsTA
NR_130706.2:n.2617-180_2617-179delinsTA