Canonical Allele Identifier: CA2080781809

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018776C= , CM000675.2:g.28018776C=	GRCh38
NC_000013.10:g.28592913C= , CM000675.1:g.28592913C=	GRCh37
NC_000013.9:g.27490913C=	NCBI36
NG_007066.1:g.86793G= , LRG_457:g.86793G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2419-187G= MANE Select	ENSP00000241453.7:n.2419-187G=
ENST00000241453.11:c.2419-187G=	ENSP00000241453.7:n.2419-187G=
ENST00000380987.2:c.*331-187G=	ENSP00000370374.2:n.*331-187G=
NM_004119.2:c.2419-187G= , LRG_457t1:c.2419-187G=	NP_004110.2:n.2419-187G=
NR_130706.1:n.2633-187G=
XM_011535015.1:c.2362-187G=	XP_011533317.1:n.2362-187G=
XM_011535016.1:c.1894-187G=	XP_011533318.1:n.1894-187G=
XM_011535017.1:c.1894-187G=	XP_011533319.1:n.1894-187G=
XM_011535018.1:c.1894-187G=	XP_011533320.1:n.1894-187G=
XM_011535015.2:c.2362-187G=	XP_011533317.1:n.2362-187G=
XM_011535017.2:c.1894-187G=	XP_011533319.1:n.1894-187G=
XM_011535018.2:c.1894-187G=	XP_011533320.1:n.1894-187G=
XM_017020486.1:c.2203-187G=	XP_016875975.1:n.2203-187G=
XM_017020487.1:c.1894-187G=	XP_016875976.1:n.1894-187G=
XM_017020488.1:c.1540-187G=	XP_016875977.1:n.1540-187G=
XM_017020489.1:c.1522-187G=	XP_016875978.1:n.1522-187G=
NM_004119.3:c.2419-187G= MANE Select	NP_004110.2:n.2419-187G=
NR_130706.2:n.2617-187G=