Canonical Allele Identifier: CA1957581359
Gene: FANCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22625492_22625493delinsCT , CM000673.2:g.22625492_22625493delinsCT GRCh38
NC_000011.9:g.22647038_22647039delinsCT , CM000673.1:g.22647038_22647039delinsCT GRCh37
NC_000011.8:g.22603614_22603615delinsCT NCBI36
NG_007425.1:g.5349_5350delinsAG , LRG_527:g.5349_5350delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000327470.6:c.318_319delinsAG MANE Select ENSP00000330875.3:p.Ala106=
ENST00000327470.4:c.318_319delinsAG ENSP00000330875.3:p.Ala106=
NM_022725.3:c.318_319delinsAG , LRG_527t1:c.318_319delinsAG NP_073562.1:p.Ala106=
NM_022725.4:c.318_319delinsAG MANE Select NP_073562.1:p.Ala106=