Canonical Allele Identifier: CA1957606958
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624990_22624994delinsTAGAC , CM000673.2:g.22624990_22624994delinsTAGAC GRCh38
NC_000011.9:g.22646536_22646540delinsTAGAC , CM000673.1:g.22646536_22646540delinsTAGAC GRCh37
NC_000011.8:g.22603112_22603116delinsTAGAC NCBI36
NG_007425.1:g.5848_5852delinsGTCTA , LRG_527:g.5848_5852delinsGTCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.817_821delinsGTCTA MANE Select ENSP00000330875.3:p.Val273=
ENST00000327470.4:c.817_821delinsGTCTA ENSP00000330875.3:p.Val273=
NM_022725.3:c.817_821delinsGTCTA , LRG_527t1:c.817_821delinsGTCTA NP_073562.1:p.Val273=
NM_022725.4:c.817_821delinsGTCTA MANE Select NP_073562.1:p.Val273=
Search 100 bp 5'
Search 100 bp 3'