Canonical Allele Identifier: CA2080781784

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018741_28018745delinsCAACA , CM000675.2:g.28018741_28018745delinsCAACA	GRCh38
NC_000013.10:g.28592878_28592882delinsCAACA , CM000675.1:g.28592878_28592882delinsCAACA	GRCh37
NC_000013.9:g.27490878_27490882delinsCAACA	NCBI36
NG_007066.1:g.86824_86828delinsTGTTG , LRG_457:g.86824_86828delinsTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-156_2419-152delinsTGTTG MANE Select	ENSP00000241453.7:n.2419-156_2419-152delinsTGTTG
ENST00000241453.11:c.2419-156_2419-152delinsTGTTG	ENSP00000241453.7:n.2419-156_2419-152delinsTGTTG
ENST00000380987.2:c.*331-156_*331-152delinsTGTTG	ENSP00000370374.2:n.*331-156_*331-152delinsTGTTG
NM_004119.2:c.2419-156_2419-152delinsTGTTG , LRG_457t1:c.2419-156_2419-152delinsTGTTG	NP_004110.2:n.2419-156_2419-152delinsTGTTG
NR_130706.1:n.2633-156_2633-152delinsTGTTG
XM_011535015.1:c.2362-156_2362-152delinsTGTTG	XP_011533317.1:n.2362-156_2362-152delinsTGTTG
XM_011535016.1:c.1894-156_1894-152delinsTGTTG	XP_011533318.1:n.1894-156_1894-152delinsTGTTG
XM_011535017.1:c.1894-156_1894-152delinsTGTTG	XP_011533319.1:n.1894-156_1894-152delinsTGTTG
XM_011535018.1:c.1894-156_1894-152delinsTGTTG	XP_011533320.1:n.1894-156_1894-152delinsTGTTG
XM_011535015.2:c.2362-156_2362-152delinsTGTTG	XP_011533317.1:n.2362-156_2362-152delinsTGTTG
XM_011535017.2:c.1894-156_1894-152delinsTGTTG	XP_011533319.1:n.1894-156_1894-152delinsTGTTG
XM_011535018.2:c.1894-156_1894-152delinsTGTTG	XP_011533320.1:n.1894-156_1894-152delinsTGTTG
XM_017020486.1:c.2203-156_2203-152delinsTGTTG	XP_016875975.1:n.2203-156_2203-152delinsTGTTG
XM_017020487.1:c.1894-156_1894-152delinsTGTTG	XP_016875976.1:n.1894-156_1894-152delinsTGTTG
XM_017020488.1:c.1540-156_1540-152delinsTGTTG	XP_016875977.1:n.1540-156_1540-152delinsTGTTG
XM_017020489.1:c.1522-156_1522-152delinsTGTTG	XP_016875978.1:n.1522-156_1522-152delinsTGTTG
NM_004119.3:c.2419-156_2419-152delinsTGTTG MANE Select	NP_004110.2:n.2419-156_2419-152delinsTGTTG
NR_130706.2:n.2617-156_2617-152delinsTGTTG