Canonical Allele Identifier: CA1957607169
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625383A= , CM000673.2:g.22625383A= GRCh38
NC_000011.9:g.22646929A= , CM000673.1:g.22646929A= GRCh37
NC_000011.8:g.22603505A= NCBI36
NG_007425.1:g.5459T= , LRG_527:g.5459T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.428T= MANE Select ENSP00000330875.3:p.Val143=
ENST00000327470.4:c.428T= ENSP00000330875.3:p.Val143=
NM_022725.3:c.428T= , LRG_527t1:c.428T= NP_073562.1:p.Val143=
NM_022725.4:c.428T= MANE Select NP_073562.1:p.Val143=