Canonical Allele Identifier: CA2790714008
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625034_22625035insCACACCCAACAC , CM000673.2:g.22625034_22625035insCACACCCAACAC GRCh38
NC_000011.9:g.22646580_22646581insCACACCCAACAC , CM000673.1:g.22646580_22646581insCACACCCAACAC GRCh37
NC_000011.8:g.22603156_22603157insCACACCCAACAC NCBI36
NG_007425.1:g.5807_5808insGTGTTGGGTGTG , LRG_527:g.5807_5808insGTGTTGGGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.776_777insGTGTTGGGTGTG MANE Select ENSP00000330875.3:p.Leu259_Leu260insCysTrpValCys
ENST00000327470.4:c.776_777insGTGTTGGGTGTG ENSP00000330875.3:p.Leu259_Leu260insCysTrpValCys
NM_022725.3:c.776_777insGTGTTGGGTGTG , LRG_527t1:c.776_777insGTGTTGGGTGTG NP_073562.1:p.Leu259_Leu260insCysTrpValCys
NM_022725.4:c.776_777insGTGTTGGGTGTG MANE Select NP_073562.1:p.Leu259_Leu260insCysTrpValCys
Search 100 bp 5'
Search 100 bp 3'