Canonical Allele Identifier: CA891842170

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034147_28034148insCCCTAGGGTGCCCTTCTCTGAAATCAACGT , CM000675.2:g.28034147_28034148insCCCTAGGGTGCCCTTCTCTGAAATCAACGT	GRCh38
NC_000013.10:g.28608284_28608285insCCCTAGGGTGCCCTTCTCTGAAATCAACGT , CM000675.1:g.28608284_28608285insCCCTAGGGTGCCCTTCTCTGAAATCAACGT	GRCh37
NC_000013.9:g.27506284_27506285insCCCTAGGGTGCCCTTCTCTGAAATCAACGT	NCBI36
NG_007066.1:g.71438_71439insGGGCACCCTAGGGACGTTGATTTCAGAGAA , LRG_457:g.71438_71439insGGGCACCCTAGGGACGTTGATTTCAGAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA MANE Select	ENSP00000241453.7:p.Glu596_Tyr597insGlyHisProArgAspValAspPheA...
ENST00000241453.11:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA	ENSP00000241453.7:p.Glu596_Tyr597insGlyHisProArgAspValAspPheA...
ENST00000380987.2:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA	ENSP00000370374.2:p.Glu596_Tyr597insGlyHisProArgAspValAspPheA...
NM_004119.2:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA , LRG_457t1:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA	NP_004110.2:p.Glu596_Tyr597insGlyHisProArgAspValAspPheArgGlu
NR_130706.1:n.1870_1871insGGGCACCCTAGGGACGTTGATTTCAGAGAA
XM_011535015.1:c.1731_1732insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533317.1:p.Glu577_Tyr578insGlyHisProArgAspValAspPheArgG...
XM_011535016.1:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533318.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_011535017.1:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533319.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_011535018.1:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533320.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_011535015.2:c.1731_1732insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533317.1:p.Glu577_Tyr578insGlyHisProArgAspValAspPheArgG...
XM_011535017.2:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533319.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_011535018.2:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_011533320.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_017020486.1:c.1572_1573insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_016875975.1:p.Glu524_Tyr525insGlyHisProArgAspValAspPheArgG...
XM_017020487.1:c.1263_1264insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_016875976.1:p.Glu421_Tyr422insGlyHisProArgAspValAspPheArgG...
XM_017020488.1:c.909_910insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_016875977.1:p.Glu303_Tyr304insGlyHisProArgAspValAspPheArgG...
XM_017020489.1:c.891_892insGGGCACCCTAGGGACGTTGATTTCAGAGAA	XP_016875978.1:p.Glu297_Tyr298insGlyHisProArgAspValAspPheArgG...
NM_004119.3:c.1788_1789insGGGCACCCTAGGGACGTTGATTTCAGAGAA MANE Select	NP_004110.2:p.Glu596_Tyr597insGlyHisProArgAspValAspPheArgGlu
NR_130706.2:n.1854_1855insGGGCACCCTAGGGACGTTGATTTCAGAGAA