Canonical Allele Identifier: CA483042253
Gene: FLT3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28592667C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018530C>T , CM000675.2:g.28018530C>T GRCh38
NC_000013.10:g.28592667C>T , CM000675.1:g.28592667C>T GRCh37
NC_000013.9:g.27490667C>T NCBI36
NG_007066.1:g.87039G>A , LRG_457:g.87039G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2478G>A MANE Select ENSP00000241453.7:p.Lys826=
ENST00000241453.11:c.2478G>A ENSP00000241453.7:p.Lys826=
ENST00000380987.2:c.*390G>A ENSP00000370374.2:n.*390G>A
NM_004119.2:c.2478G>A , LRG_457t1:c.2478G>A NP_004110.2:p.Lys826=
NR_130706.1:n.2692G>A
XM_011535015.1:c.2421G>A XP_011533317.1:p.Lys807=
XM_011535016.1:c.1953G>A XP_011533318.1:p.Lys651=
XM_011535017.1:c.1953G>A XP_011533319.1:p.Lys651=
XM_011535018.1:c.1953G>A XP_011533320.1:p.Lys651=
XM_011535015.2:c.2421G>A XP_011533317.1:p.Lys807=
XM_011535017.2:c.1953G>A XP_011533319.1:p.Lys651=
XM_011535018.2:c.1953G>A XP_011533320.1:p.Lys651=
XM_017020486.1:c.2262G>A XP_016875975.1:p.Lys754=
XM_017020487.1:c.1953G>A XP_016875976.1:p.Lys651=
XM_017020488.1:c.1599G>A XP_016875977.1:p.Lys533=
XM_017020489.1:c.1581G>A XP_016875978.1:p.Lys527=
NM_004119.3:c.2478G>A MANE Select NP_004110.2:p.Lys826=
NR_130706.2:n.2676G>A