Canonical Allele Identifier: CA2612850470
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625356-CTA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625359_22625360del , CM000673.2:g.22625359_22625360del GRCh38
NC_000011.9:g.22646905_22646906del , CM000673.1:g.22646905_22646906del GRCh37
NC_000011.8:g.22603481_22603482del NCBI36
NG_007425.1:g.5484_5485del , LRG_527:g.5484_5485del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.453_454del MANE Select ENSP00000330875.3:p.Tyr151Ter
ENST00000327470.4:c.453_454del ENSP00000330875.3:p.Tyr151Ter
NM_022725.3:c.453_454del , LRG_527t1:c.453_454del NP_073562.1:p.Tyr151Ter
NM_022725.4:c.453_454del MANE Select NP_073562.1:p.Tyr151Ter
Search 100 bp 5'
Search 100 bp 3'