Canonical Allele Identifier: CA380058158
Gene: FANCF HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.872A>C MANE Select ENSP00000330875.3:p.Lys291Thr
ENST00000327470.4:c.872A>C ENSP00000330875.3:p.Lys291Thr
NM_022725.3:c.872A>C , LRG_527t1:c.872A>C NP_073562.1:p.Lys291Thr
NM_022725.4:c.872A>C MANE Select NP_073562.1:p.Lys291Thr