Canonical Allele Identifier: CA5039687

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074971del , CM000671.2:g.35074971del	GRCh38
NC_000009.11:g.35074968del , CM000671.1:g.35074968del	GRCh37
NC_000009.10:g.35064968del	NCBI36
NG_007312.1:g.10047del , LRG_499:g.10047del
NG_007887.1:g.2773del , LRG_657:g.2773del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1593del	ENSP00000409607.2:p.Ala533ProfsTer26
ENST00000461149.2:n.2981del
ENST00000696700.1:n.3016del
ENST00000696701.1:n.1893del
ENST00000696702.1:c.*1044del	ENSP00000512821.1:n.*1044del
ENST00000696703.1:c.*977del	ENSP00000512822.1:n.*977del
ENST00000696706.1:n.1656del
ENST00000696707.1:n.1810del
ENST00000696708.1:c.*938del	ENSP00000512825.1:n.*938del
ENST00000696709.1:n.2380del
ENST00000696710.1:c.1587del	ENSP00000512826.1:p.Ala531ProfsTer26
ENST00000696711.1:n.3848del
ENST00000696712.1:n.1880del
ENST00000696713.1:c.1593del	ENSP00000512827.1:p.Ala533ProfsTer?
ENST00000696714.1:n.2173del
ENST00000696715.1:c.1593del	ENSP00000512828.1:p.Ala533ProfsTer26
ENST00000378643.8:c.1593del MANE Select	ENSP00000367910.4:p.Ala533ProfsTer26
ENST00000378643.7:c.1593del	ENSP00000367910.3:p.Ala533ProfsTer26
ENST00000425676.5:c.*1069del	ENSP00000412793.1:n.*1069del
ENST00000476212.1:n.45-538del
ENST00000481254.1:n.401del
NM_004629.1:c.1593del , LRG_499t1:c.1593del	NP_004620.1:p.Ala533ProfsTer26
NM_004629.2:c.1593del MANE Select	NP_004620.1:p.Ala533ProfsTer26