Canonical Allele Identifier: CA1957606955
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624988G= , CM000673.2:g.22624988G= GRCh38
NC_000011.9:g.22646534G= , CM000673.1:g.22646534G= GRCh37
NC_000011.8:g.22603110G= NCBI36
NG_007425.1:g.5854C= , LRG_527:g.5854C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.823C= MANE Select ENSP00000330875.3:p.Leu275=
ENST00000327470.4:c.823C= ENSP00000330875.3:p.Leu275=
NM_022725.3:c.823C= , LRG_527t1:c.823C= NP_073562.1:p.Leu275=
NM_022725.4:c.823C= MANE Select NP_073562.1:p.Leu275=
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