Canonical Allele Identifier: CA380058157
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624939T>C , CM000673.2:g.22624939T>C GRCh38
NC_000011.9:g.22646485T>C , CM000673.1:g.22646485T>C GRCh37
NC_000011.8:g.22603061T>C NCBI36
NG_007425.1:g.5903A>G , LRG_527:g.5903A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.872A>G MANE Select ENSP00000330875.3:p.Lys291Arg
ENST00000327470.4:c.872A>G ENSP00000330875.3:p.Lys291Arg
NM_022725.3:c.872A>G , LRG_527t1:c.872A>G NP_073562.1:p.Lys291Arg
NM_022725.4:c.872A>G MANE Select NP_073562.1:p.Lys291Arg