Canonical Allele Identifier: CA2831039178
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625506dup , CM000673.2:g.22625506dup GRCh38
NC_000011.9:g.22647052dup , CM000673.1:g.22647052dup GRCh37
NC_000011.8:g.22603628dup NCBI36
NG_007425.1:g.5338dup , LRG_527:g.5338dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.307dup MANE Select ENSP00000330875.3:p.Leu103ProfsTer24
ENST00000327470.4:c.307dup ENSP00000330875.3:p.Leu103ProfsTer24
NM_022725.3:c.307dup , LRG_527t1:c.307dup NP_073562.1:p.Leu103ProfsTer24
NM_022725.4:c.307dup MANE Select NP_073562.1:p.Leu103ProfsTer24
Search 100 bp 5'
Search 100 bp 3'