Canonical Allele Identifier: CA2499220871
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 1169400
ClinVar RCV Id: RCV001520576
dbSNP Id: rs2133797515
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625280del , CM000673.2:g.22625280del GRCh38
NC_000011.9:g.22646826del , CM000673.1:g.22646826del GRCh37
NC_000011.8:g.22603402del NCBI36
NG_007425.1:g.5565del , LRG_527:g.5565del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.534del MANE Select ENSP00000330875.3:p.Lys179ArgfsTer24
ENST00000327470.4:c.534del ENSP00000330875.3:p.Lys179ArgfsTer24
NM_022725.3:c.534del , LRG_527t1:c.534del NP_073562.1:p.Lys179ArgfsTer24
NM_022725.4:c.534del MANE Select NP_073562.1:p.Lys179ArgfsTer24
Search 100 bp 5'
Search 100 bp 3'