Canonical Allele Identifier: CA1957581343
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625468G= , CM000673.2:g.22625468G= GRCh38
NC_000011.9:g.22647014G= , CM000673.1:g.22647014G= GRCh37
NC_000011.8:g.22603590G= NCBI36
NG_007425.1:g.5374C= , LRG_527:g.5374C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.343C= MANE Select ENSP00000330875.3:p.Leu115=
ENST00000327470.4:c.343C= ENSP00000330875.3:p.Leu115=
NM_022725.3:c.343C= , LRG_527t1:c.343C= NP_073562.1:p.Leu115=
NM_022725.4:c.343C= MANE Select NP_073562.1:p.Leu115=
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