Canonical Allele Identifier: CA1957607079
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625206_22625207delinsAG , CM000673.2:g.22625206_22625207delinsAG GRCh38
NC_000011.9:g.22646752_22646753delinsAG , CM000673.1:g.22646752_22646753delinsAG GRCh37
NC_000011.8:g.22603328_22603329delinsAG NCBI36
NG_007425.1:g.5635_5636delinsCT , LRG_527:g.5635_5636delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.604_605delinsCT MANE Select ENSP00000330875.3:p.Leu202=
ENST00000327470.4:c.604_605delinsCT ENSP00000330875.3:p.Leu202=
NM_022725.3:c.604_605delinsCT , LRG_527t1:c.604_605delinsCT NP_073562.1:p.Leu202=
NM_022725.4:c.604_605delinsCT MANE Select NP_073562.1:p.Leu202=
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Search 100 bp 3'