Canonical Allele Identifier: CA891862822
Gene: FANCF HGNC NCBI

Linked Data

ClinVar Variation Id: 591962
ClinVar RCV Id: RCV000723145 RCV002485842 RCV002535042
dbSNP Id: rs1565055434
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625492_22625493delinsGG , CM000673.2:g.22625492_22625493delinsGG GRCh38
NC_000011.9:g.22647038_22647039delinsGG , CM000673.1:g.22647038_22647039delinsGG GRCh37
NC_000011.8:g.22603614_22603615delinsGG NCBI36
NG_007425.1:g.5349_5350delinsCC , LRG_527:g.5349_5350delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.318_319delinsCC MANE Select ENSP00000330875.3:p.Ala107Pro
ENST00000327470.4:c.318_319delinsCC ENSP00000330875.3:p.Ala107Pro
NM_022725.3:c.318_319delinsCC , LRG_527t1:c.318_319delinsCC NP_073562.1:p.Ala107Pro
NM_022725.4:c.318_319delinsCC MANE Select NP_073562.1:p.Ala107Pro
Search 100 bp 5'
Search 100 bp 3'