Canonical Allele Identifier: CA2612850472
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625462-GAA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625464_22625465del , CM000673.2:g.22625464_22625465del GRCh38
NC_000011.9:g.22647010_22647011del , CM000673.1:g.22647010_22647011del GRCh37
NC_000011.8:g.22603586_22603587del NCBI36
NG_007425.1:g.5378_5379del , LRG_527:g.5378_5379del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.347_348del MANE Select ENSP00000330875.3:p.Phe116SerfsTer10
ENST00000327470.4:c.347_348del ENSP00000330875.3:p.Phe116SerfsTer10
NM_022725.3:c.347_348del , LRG_527t1:c.347_348del NP_073562.1:p.Phe116SerfsTer10
NM_022725.4:c.347_348del MANE Select NP_073562.1:p.Phe116SerfsTer10
Search 100 bp 5'
Search 100 bp 3'