Canonical Allele Identifier: CA159813
Gene: FLT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28070610C>G , CM000675.2:g.28070610C>G GRCh38
NC_000013.10:g.28644747C>G , CM000675.1:g.28644747C>G GRCh37
NC_000013.9:g.27542747C>G NCBI36
NG_007066.1:g.34959G>C , LRG_457:g.34959G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.46G>C MANE Select ENSP00000241453.7:p.Val16Leu
ENST00000241453.11:c.46G>C ENSP00000241453.7:p.Val16Leu
ENST00000380987.2:c.46G>C ENSP00000370374.2:p.Val16Leu
NM_004119.2:c.46G>C , LRG_457t1:c.46G>C NP_004110.2:p.Val16Leu
NR_130706.1:n.128G>C
XM_011535015.1:c.-12G>C XP_011533317.1:n.-12G>C
XM_011535015.2:c.-12G>C XP_011533317.1:n.-12G>C
XM_017020486.1:c.46G>C XP_016875975.1:p.Val16Leu
XM_017020487.1:c.-572G>C XP_016875976.1:n.-572G>C
XM_017020488.1:c.-628G>C XP_016875977.1:n.-628G>C
XM_017020489.1:c.-722G>C XP_016875978.1:n.-722G>C
NM_004119.3:c.46G>C MANE Select NP_004110.2:p.Val16Leu
NR_130706.2:n.112G>C