Canonical Allele Identifier: CA2080790569

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28028142_28028144delinsCTT , CM000675.2:g.28028142_28028144delinsCTT	GRCh38
NC_000013.10:g.28602279_28602281delinsCTT , CM000675.1:g.28602279_28602281delinsCTT	GRCh37
NC_000013.9:g.27500279_27500281delinsCTT	NCBI36
NG_007066.1:g.77425_77427delinsAAG , LRG_457:g.77425_77427delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2053+34_2053+36delinsAAG MANE Select	ENSP00000241453.7:n.2053+34_2053+36delins...
ENST00000241453.11:c.2053+34_2053+36delinsAAG	ENSP00000241453.7:n.2053+34_2053+36delins...
ENST00000380987.2:c.2053+34_2053+36delinsAAG	ENSP00000370374.2:n.2053+34_2053+36delins...
NM_004119.2:c.2053+34_2053+36delinsAAG , LRG_457t1:c.2053+34_2053+36delinsAAG	NP_004110.2:n.2053+34_2053+36delinsAAG
NR_130706.1:n.2135+34_2135+36delinsAAG
XM_011535015.1:c.1996+34_1996+36delinsAAG	XP_011533317.1:n.1996+34_1996+36delinsAAG...
XM_011535016.1:c.1528+34_1528+36delinsAAG	XP_011533318.1:n.1528+34_1528+36delinsAAG...
XM_011535017.1:c.1528+34_1528+36delinsAAG	XP_011533319.1:n.1528+34_1528+36delinsAAG...
XM_011535018.1:c.1528+34_1528+36delinsAAG	XP_011533320.1:n.1528+34_1528+36delinsAAG...
XM_011535015.2:c.1996+34_1996+36delinsAAG	XP_011533317.1:n.1996+34_1996+36delinsAAG...
XM_011535017.2:c.1528+34_1528+36delinsAAG	XP_011533319.1:n.1528+34_1528+36delinsAAG...
XM_011535018.2:c.1528+34_1528+36delinsAAG	XP_011533320.1:n.1528+34_1528+36delinsAAG...
XM_017020486.1:c.1837+34_1837+36delinsAAG	XP_016875975.1:n.1837+34_1837+36delinsAAG...
XM_017020487.1:c.1528+34_1528+36delinsAAG	XP_016875976.1:n.1528+34_1528+36delinsAAG...
XM_017020488.1:c.1174+34_1174+36delinsAAG	XP_016875977.1:n.1174+34_1174+36delinsAAG...
XM_017020489.1:c.1156+34_1156+36delinsAAG	XP_016875978.1:n.1156+34_1156+36delinsAAG...
NM_004119.3:c.2053+34_2053+36delinsAAG MANE Select	NP_004110.2:n.2053+34_2053+36delinsAAG
NR_130706.2:n.2119+34_2119+36delinsAAG