Canonical Allele Identifier: CA1139660964
Gene: FANCG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35075539del , CM000671.2:g.35075539del GRCh38
NC_000009.11:g.35075536del , CM000671.1:g.35075536del GRCh37
NC_000009.10:g.35065536del NCBI36
NG_007312.1:g.9478del , LRG_499:g.9478del
NG_007887.1:g.2204del , LRG_657:g.2204del

Transcript Alleles

HGVS Amino-acid Change
ENST00000448890.2:c.1359del ENSP00000409607.2:p.Ala454ProfsTer?
ENST00000461149.2:n.2551del
ENST00000696700.1:n.2586del
ENST00000696701.1:n.1463del
ENST00000696702.1:c.*810del ENSP00000512821.1:n.*810del
ENST00000696703.1:c.*743del ENSP00000512822.1:n.*743del
ENST00000696706.1:n.1422del
ENST00000696707.1:n.1576del
ENST00000696708.1:c.*704del ENSP00000512825.1:n.*704del
ENST00000696709.1:n.1950del
ENST00000696710.1:c.1359del ENSP00000512826.1:p.Ala454ProfsTer?
ENST00000696711.1:n.3418del
ENST00000696712.1:n.1450del
ENST00000696713.1:c.1359del ENSP00000512827.1:p.Ala454ProfsTer?
ENST00000696714.1:n.1743del
ENST00000696715.1:c.1359del ENSP00000512828.1:p.Ala454ProfsTer?
ENST00000378643.8:c.1359del MANE Select ENSP00000367910.4:p.Ala454ProfsTer?
ENST00000378643.7:c.1359del ENSP00000367910.3:p.Ala454ProfsTer?
ENST00000425676.5:c.*835del ENSP00000412793.1:n.*835del
ENST00000476212.1:n.44+983del
NM_004629.1:c.1359del , LRG_499t1:c.1359del NP_004620.1:p.Ala454ProfsTer?
NM_004629.2:c.1359del MANE Select NP_004620.1:p.Ala454ProfsTer?