Canonical Allele Identifier: CA1957607021
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625111_22625113delinsTCC , CM000673.2:g.22625111_22625113delinsTCC GRCh38
NC_000011.9:g.22646657_22646659delinsTCC , CM000673.1:g.22646657_22646659delinsTCC GRCh37
NC_000011.8:g.22603233_22603235delinsTCC NCBI36
NG_007425.1:g.5729_5731delinsGGA , LRG_527:g.5729_5731delinsGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.698_700delinsGGA MANE Select ENSP00000330875.3:p.Gly233=
ENST00000327470.4:c.698_700delinsGGA ENSP00000330875.3:p.Gly233=
NM_022725.3:c.698_700delinsGGA , LRG_527t1:c.698_700delinsGGA NP_073562.1:p.Gly233=
NM_022725.4:c.698_700delinsGGA MANE Select NP_073562.1:p.Gly233=
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