Canonical Allele Identifier: CA1957607027
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625120_22625121delinsCA , CM000673.2:g.22625120_22625121delinsCA GRCh38
NC_000011.9:g.22646666_22646667delinsCA , CM000673.1:g.22646666_22646667delinsCA GRCh37
NC_000011.8:g.22603242_22603243delinsCA NCBI36
NG_007425.1:g.5721_5722delinsTG , LRG_527:g.5721_5722delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.690_691delinsTG MANE Select ENSP00000330875.3:p.Pro230=
ENST00000327470.4:c.690_691delinsTG ENSP00000330875.3:p.Pro230=
NM_022725.3:c.690_691delinsTG , LRG_527t1:c.690_691delinsTG NP_073562.1:p.Pro230=
NM_022725.4:c.690_691delinsTG MANE Select NP_073562.1:p.Pro230=
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Search 100 bp 3'