Canonical Allele Identifier: CA2080793212

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28034044G= , CM000675.2:g.28034044G=	GRCh38
NC_000013.10:g.28608181G= , CM000675.1:g.28608181G=	GRCh37
NC_000013.9:g.27506181G=	NCBI36
NG_007066.1:g.71525C= , LRG_457:g.71525C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000241453.12:c.1837+38C= MANE Select	ENSP00000241453.7:n.1837+38C=
ENST00000241453.11:c.1837+38C=	ENSP00000241453.7:n.1837+38C=
ENST00000380987.2:c.1837+38C=	ENSP00000370374.2:n.1837+38C=
NM_004119.2:c.1837+38C= , LRG_457t1:c.1837+38C=	NP_004110.2:n.1837+38C=
NR_130706.1:n.1919+38C=
XM_011535015.1:c.1780+38C=	XP_011533317.1:n.1780+38C=
XM_011535016.1:c.1312+38C=	XP_011533318.1:n.1312+38C=
XM_011535017.1:c.1312+38C=	XP_011533319.1:n.1312+38C=
XM_011535018.1:c.1312+38C=	XP_011533320.1:n.1312+38C=
XM_011535015.2:c.1780+38C=	XP_011533317.1:n.1780+38C=
XM_011535017.2:c.1312+38C=	XP_011533319.1:n.1312+38C=
XM_011535018.2:c.1312+38C=	XP_011533320.1:n.1312+38C=
XM_017020486.1:c.1621+38C=	XP_016875975.1:n.1621+38C=
XM_017020487.1:c.1312+38C=	XP_016875976.1:n.1312+38C=
XM_017020488.1:c.958+38C=	XP_016875977.1:n.958+38C=
XM_017020489.1:c.940+38C=	XP_016875978.1:n.940+38C=
NM_004119.3:c.1837+38C= MANE Select	NP_004110.2:n.1837+38C=
NR_130706.2:n.1903+38C=