Canonical Allele Identifier: CA2612850460
Gene: FANCF HGNC NCBI

Linked Data

gnomAD v4: 11-22624991-AG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624992del , CM000673.2:g.22624992del GRCh38
NC_000011.9:g.22646538del , CM000673.1:g.22646538del GRCh37
NC_000011.8:g.22603114del NCBI36
NG_007425.1:g.5850del , LRG_527:g.5850del

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.819del MANE Select ENSP00000330875.3:p.Tyr274IlefsTer5
ENST00000327470.4:c.819del ENSP00000330875.3:p.Tyr274IlefsTer5
NM_022725.3:c.819del , LRG_527t1:c.819del NP_073562.1:p.Tyr274IlefsTer5
NM_022725.4:c.819del MANE Select NP_073562.1:p.Tyr274IlefsTer5
Search 100 bp 5'
Search 100 bp 3'