Canonical Allele Identifier: CA598390432
Gene: FANCF HGNC NCBI

Linked Data

dbSNP Id: rs1309840208
gnomAD v2: 11-22646576-TCAAAAGC-T
gnomAD v4: 11-22625030-TCAAAAGC-T
MyVariant Identifiers: chr11:g.22646577_22646583del (hg19) chr11:g.22625031_22625037del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625032_22625038del , CM000673.2:g.22625032_22625038del GRCh38
NC_000011.9:g.22646578_22646584del , CM000673.1:g.22646578_22646584del GRCh37
NC_000011.8:g.22603154_22603160del NCBI36
NG_007425.1:g.5805_5811del , LRG_527:g.5805_5811del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.774_780del MANE Select ENSP00000330875.3:p.Leu260Ter
ENST00000327470.4:c.774_780del ENSP00000330875.3:p.Leu260Ter
NM_022725.3:c.774_780del , LRG_527t1:c.774_780del NP_073562.1:p.Leu260Ter
NM_022725.4:c.774_780del MANE Select NP_073562.1:p.Leu260Ter
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