Canonical Allele Identifier: CA2695196705

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028089_28028093delinsAAGAG , CM000675.2:g.28028089_28028093delinsAAGAG	GRCh38
NC_000013.10:g.28602226_28602230delinsAAGAG , CM000675.1:g.28602226_28602230delinsAAGAG	GRCh37
NC_000013.9:g.27500226_27500230delinsAAGAG	NCBI36
NG_007066.1:g.77476_77480delinsCTCTT , LRG_457:g.77476_77480delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2053+85_2053+89delinsCTCTT MANE Select	ENSP00000241453.7:n.2053+85_2053+89delinsCTCTT
ENST00000241453.11:c.2053+85_2053+89delinsCTCTT	ENSP00000241453.7:n.2053+85_2053+89delinsCTCTT
ENST00000380987.2:c.2053+85_2053+89delinsCTCTT	ENSP00000370374.2:n.2053+85_2053+89delinsCTCTT
NM_004119.2:c.2053+85_2053+89delinsCTCTT , LRG_457t1:c.2053+85_2053+89delinsCTCTT	NP_004110.2:n.2053+85_2053+89delinsCTCTT
NR_130706.1:n.2135+85_2135+89delinsCTCTT
XM_011535015.1:c.1996+85_1996+89delinsCTCTT	XP_011533317.1:n.1996+85_1996+89delinsCTCTT
XM_011535016.1:c.1528+85_1528+89delinsCTCTT	XP_011533318.1:n.1528+85_1528+89delinsCTCTT
XM_011535017.1:c.1528+85_1528+89delinsCTCTT	XP_011533319.1:n.1528+85_1528+89delinsCTCTT
XM_011535018.1:c.1528+85_1528+89delinsCTCTT	XP_011533320.1:n.1528+85_1528+89delinsCTCTT
XM_011535015.2:c.1996+85_1996+89delinsCTCTT	XP_011533317.1:n.1996+85_1996+89delinsCTCTT
XM_011535017.2:c.1528+85_1528+89delinsCTCTT	XP_011533319.1:n.1528+85_1528+89delinsCTCTT
XM_011535018.2:c.1528+85_1528+89delinsCTCTT	XP_011533320.1:n.1528+85_1528+89delinsCTCTT
XM_017020486.1:c.1837+85_1837+89delinsCTCTT	XP_016875975.1:n.1837+85_1837+89delinsCTCTT
XM_017020487.1:c.1528+85_1528+89delinsCTCTT	XP_016875976.1:n.1528+85_1528+89delinsCTCTT
XM_017020488.1:c.1174+85_1174+89delinsCTCTT	XP_016875977.1:n.1174+85_1174+89delinsCTCTT
XM_017020489.1:c.1156+85_1156+89delinsCTCTT	XP_016875978.1:n.1156+85_1156+89delinsCTCTT
NM_004119.3:c.2053+85_2053+89delinsCTCTT MANE Select	NP_004110.2:n.2053+85_2053+89delinsCTCTT
NR_130706.2:n.2119+85_2119+89delinsCTCTT