Canonical Allele Identifier: CA2695213428
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625417_22625454del , CM000673.2:g.22625417_22625454del GRCh38
NC_000011.9:g.22646963_22647000del , CM000673.1:g.22646963_22647000del GRCh37
NC_000011.8:g.22603539_22603576del NCBI36
NG_007425.1:g.5389_5426del , LRG_527:g.5389_5426del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.358_395del MANE Select ENSP00000330875.3:p.Gly120ProfsTer20
ENST00000327470.4:c.358_395del ENSP00000330875.3:p.Gly120ProfsTer20
NM_022725.3:c.358_395del , LRG_527t1:c.358_395del NP_073562.1:p.Gly120ProfsTer20
NM_022725.4:c.358_395del MANE Select NP_073562.1:p.Gly120ProfsTer20