Canonical Allele Identifier: CA2612850465
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625233-C-CT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625233_22625234insT , CM000673.2:g.22625233_22625234insT GRCh38
NC_000011.9:g.22646779_22646780insT , CM000673.1:g.22646779_22646780insT GRCh37
NC_000011.8:g.22603355_22603356insT NCBI36
NG_007425.1:g.5608_5609insA , LRG_527:g.5608_5609insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.577_578insA MANE Select ENSP00000330875.3:p.Trp193Ter
ENST00000327470.4:c.577_578insA ENSP00000330875.3:p.Trp193Ter
NM_022725.3:c.577_578insA , LRG_527t1:c.577_578insA NP_073562.1:p.Trp193Ter
NM_022725.4:c.577_578insA MANE Select NP_073562.1:p.Trp193Ter
Search 100 bp 5'
Search 100 bp 3'