Canonical Allele Identifier: CA1957606921
Gene: FANCF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22624921_22624922delinsGT , CM000673.2:g.22624921_22624922delinsGT GRCh38
NC_000011.9:g.22646467_22646468delinsGT , CM000673.1:g.22646467_22646468delinsGT GRCh37
NC_000011.8:g.22603043_22603044delinsGT NCBI36
NG_007425.1:g.5920_5921delinsAC , LRG_527:g.5920_5921delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000327470.6:c.889_890delinsAC MANE Select ENSP00000330875.3:p.Thr297=
ENST00000327470.4:c.889_890delinsAC ENSP00000330875.3:p.Thr297=
NM_022725.3:c.889_890delinsAC , LRG_527t1:c.889_890delinsAC NP_073562.1:p.Thr297=
NM_022725.4:c.889_890delinsAC MANE Select NP_073562.1:p.Thr297=
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