Canonical Allele Identifier: CA2080781422

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018497_28018500delinsCATG , CM000675.2:g.28018497_28018500delinsCATG	GRCh38
NC_000013.10:g.28592634_28592637delinsCATG , CM000675.1:g.28592634_28592637delinsCATG	GRCh37
NC_000013.9:g.27490634_27490637delinsCATG	NCBI36
NG_007066.1:g.87069_87072delinsCATG , LRG_457:g.87069_87072delinsCATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.2508_2511delinsCATG MANE Select	ENSP00000241453.7:p.Ile836=
ENST00000241453.11:c.2508_2511delinsCATG	ENSP00000241453.7:p.Ile836=
ENST00000380987.2:c.*420_*423delinsCATG	ENSP00000370374.2:n.*420_*423delinsCATG
NM_004119.2:c.2508_2511delinsCATG , LRG_457t1:c.2508_2511delinsCATG	NP_004110.2:p.Ile836=
NR_130706.1:n.2722_2725delinsCATG
XM_011535015.1:c.2451_2454delinsCATG	XP_011533317.1:p.Ile817=
XM_011535016.1:c.1983_1986delinsCATG	XP_011533318.1:p.Ile661=
XM_011535017.1:c.1983_1986delinsCATG	XP_011533319.1:p.Ile661=
XM_011535018.1:c.1983_1986delinsCATG	XP_011533320.1:p.Ile661=
XM_011535015.2:c.2451_2454delinsCATG	XP_011533317.1:p.Ile817=
XM_011535017.2:c.1983_1986delinsCATG	XP_011533319.1:p.Ile661=
XM_011535018.2:c.1983_1986delinsCATG	XP_011533320.1:p.Ile661=
XM_017020486.1:c.2292_2295delinsCATG	XP_016875975.1:p.Ile764=
XM_017020487.1:c.1983_1986delinsCATG	XP_016875976.1:p.Ile661=
XM_017020488.1:c.1629_1632delinsCATG	XP_016875977.1:p.Ile543=
XM_017020489.1:c.1611_1614delinsCATG	XP_016875978.1:p.Ile537=
NM_004119.3:c.2508_2511delinsCATG MANE Select	NP_004110.2:p.Ile836=
NR_130706.2:n.2706_2709delinsCATG