Canonical Allele Identifier: CA387650213
Community Standard Title: NM_004119.3(FLT3):c.2495T>G (p.Leu832Trp)
Gene: FLT3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018513A>C , CM000675.2:g.28018513A>C GRCh38
NC_000013.10:g.28592650A>C , CM000675.1:g.28592650A>C GRCh37
NC_000013.9:g.27490650A>C NCBI36
NG_007066.1:g.87056T>G , LRG_457:g.87056T>G

Transcript Alleles

HGVS Amino-acid Change
NM_004119.3:c.2495T>G MANE Select NP_004110.2:p.Leu832Trp
ENST00000241453.12:c.2495T>G MANE Select ENSP00000241453.7:p.Leu832Trp
NM_004119.2:c.2495T>G , LRG_457t1:c.2495T>G NP_004110.2:p.Leu832Trp
NR_130706.1:n.2709T>G
NR_130706.2:n.2693T>G
ENST00000241453.11:c.2495T>G ENSP00000241453.7:p.Leu832Trp
ENST00000380987.2:c.*407T>G ENSP00000370374.2:n.*407T>G
XM_011535015.1:c.2438T>G XP_011533317.1:p.Leu813Trp
XM_011535015.2:c.2438T>G XP_011533317.1:p.Leu813Trp
XM_011535016.1:c.1970T>G XP_011533318.1:p.Leu657Trp
XM_011535017.1:c.1970T>G XP_011533319.1:p.Leu657Trp
XM_011535017.2:c.1970T>G XP_011533319.1:p.Leu657Trp
XM_011535018.1:c.1970T>G XP_011533320.1:p.Leu657Trp
XM_011535018.2:c.1970T>G XP_011533320.1:p.Leu657Trp
XM_017020486.1:c.2279T>G XP_016875975.1:p.Leu760Trp
XM_017020487.1:c.1970T>G XP_016875976.1:p.Leu657Trp
XM_017020488.1:c.1616T>G XP_016875977.1:p.Leu539Trp
XM_017020489.1:c.1598T>G XP_016875978.1:p.Leu533Trp
Search 100 bp 5'
Search 100 bp 3'