Canonical Allele Identifier: CA645598015

Gene: FLT3

Linked Data

• COSMIC: COSM303807

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034147_28034149del , CM000675.2:g.28034147_28034149del	GRCh38
NC_000013.10:g.28608284_28608286del , CM000675.1:g.28608284_28608286del	GRCh37
NC_000013.9:g.27506284_27506286del	NCBI36
NG_007066.1:g.71421_71423del , LRG_457:g.71421_71423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.1771_1773del MANE Select	ENSP00000241453.7:p.Tyr591del
ENST00000241453.11:c.1771_1773del	ENSP00000241453.7:p.Tyr591del
ENST00000380987.2:c.1771_1773del	ENSP00000370374.2:p.Tyr591del
NM_004119.2:c.1771_1773del , LRG_457t1:c.1771_1773del	NP_004110.2:p.Tyr591del
NR_130706.1:n.1853_1855del
XM_011535015.1:c.1714_1716del	XP_011533317.1:p.Tyr572del
XM_011535016.1:c.1246_1248del	XP_011533318.1:p.Tyr416del
XM_011535017.1:c.1246_1248del	XP_011533319.1:p.Tyr416del
XM_011535018.1:c.1246_1248del	XP_011533320.1:p.Tyr416del
XM_011535015.2:c.1714_1716del	XP_011533317.1:p.Tyr572del
XM_011535017.2:c.1246_1248del	XP_011533319.1:p.Tyr416del
XM_011535018.2:c.1246_1248del	XP_011533320.1:p.Tyr416del
XM_017020486.1:c.1555_1557del	XP_016875975.1:p.Tyr519del
XM_017020487.1:c.1246_1248del	XP_016875976.1:p.Tyr416del
XM_017020488.1:c.892_894del	XP_016875977.1:p.Tyr298del
XM_017020489.1:c.874_876del	XP_016875978.1:p.Tyr292del
NM_004119.3:c.1771_1773del MANE Select	NP_004110.2:p.Tyr591del
NR_130706.2:n.1837_1839del