Canonical Allele Identifier: CA1957607142
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625325_22625327delinsCAG , CM000673.2:g.22625325_22625327delinsCAG GRCh38
NC_000011.9:g.22646871_22646873delinsCAG , CM000673.1:g.22646871_22646873delinsCAG GRCh37
NC_000011.8:g.22603447_22603449delinsCAG NCBI36
NG_007425.1:g.5515_5517delinsCTG , LRG_527:g.5515_5517delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.484_486delinsCTG MANE Select ENSP00000330875.3:p.Leu162=
ENST00000327470.4:c.484_486delinsCTG ENSP00000330875.3:p.Leu162=
NM_022725.3:c.484_486delinsCTG , LRG_527t1:c.484_486delinsCTG NP_073562.1:p.Leu162=
NM_022725.4:c.484_486delinsCTG MANE Select NP_073562.1:p.Leu162=
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