Canonical Allele Identifier: CA6928315

Gene: FLT3

Linked Data

• ClinVar Variation Id: 725869
• ClinVar RCV Id: RCV000900002
• dbSNP Id: rs369177963
• ExAC: 13:28592697 G / A
• gnomAD v2: 13-28592697-G-A
• gnomAD v3: 13-28018560-G-A
• gnomAD v4: 13-28018560-G-A
• MyVariant Identifiers: chr13:g.28592697G>A (hg19) ; chr13:g.28018560G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241453.12:c.2448C>T MANE Select	ENSP00000241453.7:p.Asn816=
ENST00000241453.11:c.2448C>T	ENSP00000241453.7:p.Asn816=
ENST00000380987.2:c.*360C>T	ENSP00000370374.2:n.*360C>T
NM_004119.2:c.2448C>T , LRG_457t1:c.2448C>T	NP_004110.2:p.Asn816=
NR_130706.1:n.2662C>T
XM_011535015.1:c.2391C>T	XP_011533317.1:p.Asn797=
XM_011535016.1:c.1923C>T	XP_011533318.1:p.Asn641=
XM_011535017.1:c.1923C>T	XP_011533319.1:p.Asn641=
XM_011535018.1:c.1923C>T	XP_011533320.1:p.Asn641=
XM_011535015.2:c.2391C>T	XP_011533317.1:p.Asn797=
XM_011535017.2:c.1923C>T	XP_011533319.1:p.Asn641=
XM_011535018.2:c.1923C>T	XP_011533320.1:p.Asn641=
XM_017020486.1:c.2232C>T	XP_016875975.1:p.Asn744=
XM_017020487.1:c.1923C>T	XP_016875976.1:p.Asn641=
XM_017020488.1:c.1569C>T	XP_016875977.1:p.Asn523=
XM_017020489.1:c.1551C>T	XP_016875978.1:p.Asn517=
NM_004119.3:c.2448C>T MANE Select	NP_004110.2:p.Asn816=
NR_130706.2:n.2646C>T