Canonical Allele Identifier: CA1957606965
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625004C= , CM000673.2:g.22625004C= GRCh38
NC_000011.9:g.22646550C= , CM000673.1:g.22646550C= GRCh37
NC_000011.8:g.22603126C= NCBI36
NG_007425.1:g.5838G= , LRG_527:g.5838G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.807G= MANE Select ENSP00000330875.3:p.Ala269=
ENST00000327470.4:c.807G= ENSP00000330875.3:p.Ala269=
NM_022725.3:c.807G= , LRG_527t1:c.807G= NP_073562.1:p.Ala269=
NM_022725.4:c.807G= MANE Select NP_073562.1:p.Ala269=