Canonical Allele Identifier: CA2612849538
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22623989-TCA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22623990_22623991del , CM000673.2:g.22623990_22623991del GRCh38
NC_000011.9:g.22645536_22645537del , CM000673.1:g.22645536_22645537del GRCh37
NC_000011.8:g.22602112_22602113del NCBI36
NG_007425.1:g.6851_6852del , LRG_527:g.6851_6852del

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.*695_*696del MANE Select ENSP00000330875.3:n.*695_*696del
ENST00000327470.4:c.*695_*696del ENSP00000330875.3:n.*695_*696del
NM_022725.3:c.*695_*696del , LRG_527t1:c.*695_*696del NP_073562.1:n.*695_*696del
NM_022725.4:c.*695_*696del MANE Select NP_073562.1:n.*695_*696del
Search 100 bp 5'
Search 100 bp 3'