Canonical Allele Identifier: CA1139660947

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074383del , CM000671.2:g.35074383del	GRCh38
NC_000009.11:g.35074380del , CM000671.1:g.35074380del	GRCh37
NC_000009.10:g.35064380del	NCBI36
NG_007312.1:g.10635del , LRG_499:g.10635del
NG_007887.1:g.3361del , LRG_657:g.3361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1749del	ENSP00000409607.2:p.Asp584MetfsTer10
ENST00000461149.2:n.3569del
ENST00000696700.1:n.3604del
ENST00000696701.1:n.2049del
ENST00000696702.1:c.*1200del	ENSP00000512821.1:n.*1200del
ENST00000696703.1:c.*1133del	ENSP00000512822.1:n.*1133del
ENST00000696706.1:n.1812del
ENST00000696707.1:n.1966del
ENST00000696708.1:c.*1094del	ENSP00000512825.1:n.*1094del
ENST00000696709.1:n.2968del
ENST00000696710.1:c.1743del	ENSP00000512826.1:p.Asp582MetfsTer10
ENST00000696711.1:n.4436del
ENST00000696712.1:n.2468del
ENST00000696713.1:c.*52del	ENSP00000512827.1:n.*52del
ENST00000696714.1:n.2761del
ENST00000696715.1:c.1749del	ENSP00000512828.1:p.Asp584MetfsTer20
ENST00000378643.8:c.1749del MANE Select	ENSP00000367910.4:p.Asp584MetfsTer10
ENST00000378643.7:c.1749del	ENSP00000367910.3:p.Asp584MetfsTer10
ENST00000425676.5:c.*1225del	ENSP00000412793.1:n.*1225del
ENST00000476212.1:n.95del
NM_004629.1:c.1749del , LRG_499t1:c.1749del	NP_004620.1:p.Asp584MetfsTer10
NM_004629.2:c.1749del MANE Select	NP_004620.1:p.Asp584MetfsTer10