Canonical Allele Identifier: CA6928950

Gene: FLT3

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28061888G>C , CM000675.2:g.28061888G>C	GRCh38
NC_000013.10:g.28636025G>C , CM000675.1:g.28636025G>C	GRCh37
NC_000013.9:g.27534025G>C	NCBI36
NG_007066.1:g.43681C>G , LRG_457:g.43681C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.347C>G MANE Select	ENSP00000241453.7:p.Pro116Arg
ENST00000241453.11:c.347C>G	ENSP00000241453.7:p.Pro116Arg
ENST00000380987.2:c.347C>G	ENSP00000370374.2:p.Pro116Arg
NM_004119.2:c.347C>G , LRG_457t1:c.347C>G	NP_004110.2:p.Pro116Arg
NR_130706.1:n.429C>G
XM_011535015.1:c.290C>G	XP_011533317.1:p.Pro97Arg
XM_011535015.2:c.290C>G	XP_011533317.1:p.Pro97Arg
XM_011535017.2:c.-258C>G	XP_011533319.1:n.-258C>G
XM_017020486.1:c.347C>G	XP_016875975.1:p.Pro116Arg
XM_017020487.1:c.-271C>G	XP_016875976.1:n.-271C>G
XM_017020488.1:c.-327C>G	XP_016875977.1:n.-327C>G
XM_017020489.1:c.-421C>G	XP_016875978.1:n.-421C>G
NM_004119.3:c.347C>G MANE Select	NP_004110.2:p.Pro116Arg
NR_130706.2:n.413C>G