Canonical Allele Identifier: CA645594347
Gene: FANCF HGNC NCBI

Linked Data

COSMIC: COSM5225390
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624933dup , CM000673.2:g.22624933dup GRCh38
NC_000011.9:g.22646479dup , CM000673.1:g.22646479dup GRCh37
NC_000011.8:g.22603055dup NCBI36
NG_007425.1:g.5911dup , LRG_527:g.5911dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.880dup MANE Select ENSP00000330875.3:p.Trp294LeufsTer5
ENST00000327470.4:c.880dup ENSP00000330875.3:p.Trp294LeufsTer5
NM_022725.3:c.880dup , LRG_527t1:c.880dup NP_073562.1:p.Trp294LeufsTer5
NM_022725.4:c.880dup MANE Select NP_073562.1:p.Trp294LeufsTer5
Search 100 bp 5'
Search 100 bp 3'