Canonical Allele Identifier: CA387650333

Gene: FLT3

Linked Data

• dbSNP Id: rs2137624040
• MyVariant Identifiers: chr13:g.28592707G>C (hg19) ; chr13:g.28018570G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018570G>C , CM000675.2:g.28018570G>C	GRCh38
NC_000013.10:g.28592707G>C , CM000675.1:g.28592707G>C	GRCh37
NC_000013.9:g.27490707G>C	NCBI36
NG_007066.1:g.86999C>G , LRG_457:g.86999C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2438C>G MANE Select	ENSP00000241453.7:p.Ala813Gly
ENST00000241453.11:c.2438C>G	ENSP00000241453.7:p.Ala813Gly
ENST00000380987.2:c.*350C>G	ENSP00000370374.2:n.*350C>G
NM_004119.2:c.2438C>G , LRG_457t1:c.2438C>G	NP_004110.2:p.Ala813Gly
NR_130706.1:n.2652C>G
XM_011535015.1:c.2381C>G	XP_011533317.1:p.Ala794Gly
XM_011535016.1:c.1913C>G	XP_011533318.1:p.Ala638Gly
XM_011535017.1:c.1913C>G	XP_011533319.1:p.Ala638Gly
XM_011535018.1:c.1913C>G	XP_011533320.1:p.Ala638Gly
XM_011535015.2:c.2381C>G	XP_011533317.1:p.Ala794Gly
XM_011535017.2:c.1913C>G	XP_011533319.1:p.Ala638Gly
XM_011535018.2:c.1913C>G	XP_011533320.1:p.Ala638Gly
XM_017020486.1:c.2222C>G	XP_016875975.1:p.Ala741Gly
XM_017020487.1:c.1913C>G	XP_016875976.1:p.Ala638Gly
XM_017020488.1:c.1559C>G	XP_016875977.1:p.Ala520Gly
XM_017020489.1:c.1541C>G	XP_016875978.1:p.Ala514Gly
NM_004119.3:c.2438C>G MANE Select	NP_004110.2:p.Ala813Gly
NR_130706.2:n.2636C>G