Canonical Allele Identifier: CA2727715797
Gene: FLT3 HGNC NCBI

Linked Data

dbSNP Id: rs2137625005

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018653C>A , CM000675.2:g.28018653C>A GRCh38
NC_000013.10:g.28592790C>A , CM000675.1:g.28592790C>A GRCh37
NC_000013.9:g.27490790C>A NCBI36
NG_007066.1:g.86916G>T , LRG_457:g.86916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2419-64G>T MANE Select ENSP00000241453.7:n.2419-64G>T
ENST00000241453.11:c.2419-64G>T ENSP00000241453.7:n.2419-64G>T
ENST00000380987.2:c.*331-64G>T ENSP00000370374.2:n.*331-64G>T
NM_004119.2:c.2419-64G>T , LRG_457t1:c.2419-64G>T NP_004110.2:n.2419-64G>T
NR_130706.1:n.2633-64G>T
XM_011535015.1:c.2362-64G>T XP_011533317.1:n.2362-64G>T
XM_011535016.1:c.1894-64G>T XP_011533318.1:n.1894-64G>T
XM_011535017.1:c.1894-64G>T XP_011533319.1:n.1894-64G>T
XM_011535018.1:c.1894-64G>T XP_011533320.1:n.1894-64G>T
XM_011535015.2:c.2362-64G>T XP_011533317.1:n.2362-64G>T
XM_011535017.2:c.1894-64G>T XP_011533319.1:n.1894-64G>T
XM_011535018.2:c.1894-64G>T XP_011533320.1:n.1894-64G>T
XM_017020486.1:c.2203-64G>T XP_016875975.1:n.2203-64G>T
XM_017020487.1:c.1894-64G>T XP_016875976.1:n.1894-64G>T
XM_017020488.1:c.1540-64G>T XP_016875977.1:n.1540-64G>T
XM_017020489.1:c.1522-64G>T XP_016875978.1:n.1522-64G>T
NM_004119.3:c.2419-64G>T MANE Select NP_004110.2:n.2419-64G>T
NR_130706.2:n.2617-64G>T