Canonical Allele Identifier: CA2790714007
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625035_22625036insCCAAACACACCCAACACA , CM000673.2:g.22625035_22625036insCCAAACACACCCAACACA GRCh38
NC_000011.9:g.22646581_22646582insCCAAACACACCCAACACA , CM000673.1:g.22646581_22646582insCCAAACACACCCAACACA GRCh37
NC_000011.8:g.22603157_22603158insCCAAACACACCCAACACA NCBI36
NG_007425.1:g.5807_5808insGTGTTGGGTGTGTTTGGT , LRG_527:g.5807_5808insGTGTTGGGTGTGTTTGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.776_777insGTGTTGGGTGTGTTTGGT MANE Select ENSP00000330875.3:p.Leu259_Leu260insCysTrpValCysLeuVal
ENST00000327470.4:c.776_777insGTGTTGGGTGTGTTTGGT ENSP00000330875.3:p.Leu259_Leu260insCysTrpValCysLeuVal
NM_022725.3:c.776_777insGTGTTGGGTGTGTTTGGT , LRG_527t1:c.776_777insGTGTTGGGTGTGTTTGGT NP_073562.1:p.Leu259_Leu260insCysTrpValCysLeuVal
NM_022725.4:c.776_777insGTGTTGGGTGTGTTTGGT MANE Select NP_073562.1:p.Leu259_Leu260insCysTrpValCysLeuVal
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