Canonical Allele Identifier: CA1957607178

Gene: FANCF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22625397G= , CM000673.2:g.22625397G=	GRCh38
NC_000011.9:g.22646943G= , CM000673.1:g.22646943G=	GRCh37
NC_000011.8:g.22603519G=	NCBI36
NG_007425.1:g.5445C= , LRG_527:g.5445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.414C= MANE Select	ENSP00000330875.3:p.Arg138=
ENST00000327470.4:c.414C=	ENSP00000330875.3:p.Arg138=
NM_022725.3:c.414C= , LRG_527t1:c.414C=	NP_073562.1:p.Arg138=
NM_022725.4:c.414C= MANE Select	NP_073562.1:p.Arg138=