Canonical Allele Identifier: CA2612850471
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22625403-AAGGCGGGCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625408_22625416del , CM000673.2:g.22625408_22625416del GRCh38
NC_000011.9:g.22646954_22646962del , CM000673.1:g.22646954_22646962del GRCh37
NC_000011.8:g.22603530_22603538del NCBI36
NG_007425.1:g.5430_5438del , LRG_527:g.5430_5438del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.399_407del MANE Select ENSP00000330875.3:p.Ala134_Leu136del
ENST00000327470.4:c.399_407del ENSP00000330875.3:p.Ala134_Leu136del
NM_022725.3:c.399_407del , LRG_527t1:c.399_407del NP_073562.1:p.Ala134_Leu136del
NM_022725.4:c.399_407del MANE Select NP_073562.1:p.Ala134_Leu136del
Search 100 bp 5'
Search 100 bp 3'