Canonical Allele Identifier: CA6928302
Gene: FLT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 376723
ClinVar RCV Id: RCV000440005
dbSNP Id: rs772061268
COSMIC: COSM24666

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28018487T>G , CM000675.2:g.28018487T>G GRCh38
NC_000013.10:g.28592624T>G , CM000675.1:g.28592624T>G GRCh37
NC_000013.9:g.27490624T>G NCBI36
NG_007066.1:g.87082A>C , LRG_457:g.87082A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000241453.12:c.2521A>C MANE Select ENSP00000241453.7:p.Asn841His
ENST00000241453.11:c.2521A>C ENSP00000241453.7:p.Asn841His
ENST00000380987.2:c.*433A>C ENSP00000370374.2:n.*433A>C
NM_004119.2:c.2521A>C , LRG_457t1:c.2521A>C NP_004110.2:p.Asn841His
NR_130706.1:n.2735A>C
XM_011535015.1:c.2464A>C XP_011533317.1:p.Asn822His
XM_011535016.1:c.1996A>C XP_011533318.1:p.Asn666His
XM_011535017.1:c.1996A>C XP_011533319.1:p.Asn666His
XM_011535018.1:c.1996A>C XP_011533320.1:p.Asn666His
XM_011535015.2:c.2464A>C XP_011533317.1:p.Asn822His
XM_011535017.2:c.1996A>C XP_011533319.1:p.Asn666His
XM_011535018.2:c.1996A>C XP_011533320.1:p.Asn666His
XM_017020486.1:c.2305A>C XP_016875975.1:p.Asn769His
XM_017020487.1:c.1996A>C XP_016875976.1:p.Asn666His
XM_017020488.1:c.1642A>C XP_016875977.1:p.Asn548His
XM_017020489.1:c.1624A>C XP_016875978.1:p.Asn542His
NM_004119.3:c.2521A>C MANE Select NP_004110.2:p.Asn841His
NR_130706.2:n.2719A>C