Canonical Allele Identifier: CA387650314

Gene: FLT3

Linked Data

• MyVariant Identifiers: chr13:g.28592697G>T (hg19) ; chr13:g.28018560G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28018560G>T , CM000675.2:g.28018560G>T	GRCh38
NC_000013.10:g.28592697G>T , CM000675.1:g.28592697G>T	GRCh37
NC_000013.9:g.27490697G>T	NCBI36
NG_007066.1:g.87009C>A , LRG_457:g.87009C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2448C>A MANE Select	ENSP00000241453.7:p.Asn816Lys
ENST00000241453.11:c.2448C>A	ENSP00000241453.7:p.Asn816Lys
ENST00000380987.2:c.*360C>A	ENSP00000370374.2:n.*360C>A
NM_004119.2:c.2448C>A , LRG_457t1:c.2448C>A	NP_004110.2:p.Asn816Lys
NR_130706.1:n.2662C>A
XM_011535015.1:c.2391C>A	XP_011533317.1:p.Asn797Lys
XM_011535016.1:c.1923C>A	XP_011533318.1:p.Asn641Lys
XM_011535017.1:c.1923C>A	XP_011533319.1:p.Asn641Lys
XM_011535018.1:c.1923C>A	XP_011533320.1:p.Asn641Lys
XM_011535015.2:c.2391C>A	XP_011533317.1:p.Asn797Lys
XM_011535017.2:c.1923C>A	XP_011533319.1:p.Asn641Lys
XM_011535018.2:c.1923C>A	XP_011533320.1:p.Asn641Lys
XM_017020486.1:c.2232C>A	XP_016875975.1:p.Asn744Lys
XM_017020487.1:c.1923C>A	XP_016875976.1:p.Asn641Lys
XM_017020488.1:c.1569C>A	XP_016875977.1:p.Asn523Lys
XM_017020489.1:c.1551C>A	XP_016875978.1:p.Asn517Lys
NM_004119.3:c.2448C>A MANE Select	NP_004110.2:p.Asn816Lys
NR_130706.2:n.2646C>A