Canonical Allele Identifier: CA1957607126
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625291G= , CM000673.2:g.22625291G= GRCh38
NC_000011.9:g.22646837G= , CM000673.1:g.22646837G= GRCh37
NC_000011.8:g.22603413G= NCBI36
NG_007425.1:g.5551C= , LRG_527:g.5551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.520C= MANE Select ENSP00000330875.3:p.Leu174=
ENST00000327470.4:c.520C= ENSP00000330875.3:p.Leu174=
NM_022725.3:c.520C= , LRG_527t1:c.520C= NP_073562.1:p.Leu174=
NM_022725.4:c.520C= MANE Select NP_073562.1:p.Leu174=