Canonical Allele Identifier: CA2612850469

Gene: FANCF

Linked Data

• gnomAD v4: 11-22625350-TTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22625356_22625357del , CM000673.2:g.22625356_22625357del	GRCh38
NC_000011.9:g.22646902_22646903del , CM000673.1:g.22646902_22646903del	GRCh37
NC_000011.8:g.22603478_22603479del	NCBI36
NG_007425.1:g.5490_5491del , LRG_527:g.5490_5491del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327470.6:c.459_460del MANE Select	ENSP00000330875.3:p.Asn154ProfsTer?
ENST00000327470.4:c.459_460del	ENSP00000330875.3:p.Asn154ProfsTer?
NM_022725.3:c.459_460del , LRG_527t1:c.459_460del	NP_073562.1:p.Asn154ProfsTer?
NM_022725.4:c.459_460del MANE Select	NP_073562.1:p.Asn154ProfsTer?