Canonical Allele Identifier: CA2612850473
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625496dup , CM000673.2:g.22625496dup GRCh38
NC_000011.9:g.22647042dup , CM000673.1:g.22647042dup GRCh37
NC_000011.8:g.22603618dup NCBI36
NG_007425.1:g.5346dup , LRG_527:g.5346dup

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.315dup MANE Select ENSP00000330875.3:p.Ala106CysfsTer21
ENST00000327470.4:c.315dup ENSP00000330875.3:p.Ala106CysfsTer21
NM_022725.3:c.315dup , LRG_527t1:c.315dup NP_073562.1:p.Ala106CysfsTer21
NM_022725.4:c.315dup MANE Select NP_073562.1:p.Ala106CysfsTer21