Canonical Allele Identifier: CA2080781370

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018484A= , CM000675.2:g.28018484A=	GRCh38
NC_000013.10:g.28592621A= , CM000675.1:g.28592621A=	GRCh37
NC_000013.9:g.27490621A=	NCBI36
NG_007066.1:g.87085T= , LRG_457:g.87085T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004119.3:c.2524T= MANE Select	NP_004110.2:p.Tyr842=
ENST00000241453.12:c.2524T= MANE Select	ENSP00000241453.7:p.Tyr842=
NM_004119.2:c.2524T= , LRG_457t1:c.2524T=	NP_004110.2:p.Tyr842=
NR_130706.1:n.2738T=
NR_130706.2:n.2722T=
ENST00000241453.11:c.2524T=	ENSP00000241453.7:p.Tyr842=
ENST00000380987.2:c.*436T=	ENSP00000370374.2:n.*436T=
XM_011535015.1:c.2467T=	XP_011533317.1:p.Tyr823=
XM_011535015.2:c.2467T=	XP_011533317.1:p.Tyr823=
XM_011535016.1:c.1999T=	XP_011533318.1:p.Tyr667=
XM_011535017.1:c.1999T=	XP_011533319.1:p.Tyr667=
XM_011535017.2:c.1999T=	XP_011533319.1:p.Tyr667=
XM_011535018.1:c.1999T=	XP_011533320.1:p.Tyr667=
XM_011535018.2:c.1999T=	XP_011533320.1:p.Tyr667=
XM_017020486.1:c.2308T=	XP_016875975.1:p.Tyr770=
XM_017020487.1:c.1999T=	XP_016875976.1:p.Tyr667=
XM_017020488.1:c.1645T=	XP_016875977.1:p.Tyr549=
XM_017020489.1:c.1627T=	XP_016875978.1:p.Tyr543=