Canonical Allele Identifier: CA6928923

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28057339G>A , CM000675.2:g.28057339G>A	GRCh38
NC_000013.10:g.28631476G>A , CM000675.1:g.28631476G>A	GRCh37
NC_000013.9:g.27529476G>A	NCBI36
NG_007066.1:g.48230C>T , LRG_457:g.48230C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004119.3:c.484+8C>T MANE Select	NP_004110.2:n.484+8C>T
ENST00000241453.12:c.484+8C>T MANE Select	ENSP00000241453.7:n.484+8C>T
NM_004119.2:c.484+8C>T , LRG_457t1:c.484+8C>T	NP_004110.2:n.484+8C>T
NR_130706.1:n.566+8C>T
NR_130706.2:n.550+8C>T
ENST00000241453.11:c.484+8C>T	ENSP00000241453.7:n.484+8C>T
ENST00000380987.2:c.484+8C>T	ENSP00000370374.2:n.484+8C>T
XM_011535015.1:c.427+8C>T	XP_011533317.1:n.427+8C>T
XM_011535015.2:c.427+8C>T	XP_011533317.1:n.427+8C>T
XM_011535016.1:c.-134+8C>T	XP_011533318.1:n.-134+8C>T
XM_011535017.1:c.-134+21C>T	XP_011533319.1:n.-134+21C>T
XM_011535017.2:c.-134+21C>T	XP_011533319.1:n.-134+21C>T
XM_011535018.1:c.-42+21C>T	XP_011533320.1:n.-42+21C>T
XM_011535018.2:c.-42+21C>T	XP_011533320.1:n.-42+21C>T
XM_017020486.1:c.484+8C>T	XP_016875975.1:n.484+8C>T
XM_017020487.1:c.-134+8C>T	XP_016875976.1:n.-134+8C>T
XM_017020488.1:c.-190+8C>T	XP_016875977.1:n.-190+8C>T
XM_017020489.1:c.-284+8C>T	XP_016875978.1:n.-284+8C>T