Canonical Allele Identifier: CA373303866

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074978G>A , CM000671.2:g.35074978G>A	GRCh38
NC_000009.11:g.35074975G>A , CM000671.1:g.35074975G>A	GRCh37
NC_000009.10:g.35064975G>A	NCBI36
NG_007312.1:g.10039C>T , LRG_499:g.10039C>T
NG_007887.1:g.2765C>T , LRG_657:g.2765C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1585C>T MANE Select	NP_004620.1:p.Gln529Ter
ENST00000378643.8:c.1585C>T MANE Select	ENSP00000367910.4:p.Gln529Ter
NM_004629.1:c.1585C>T , LRG_499t1:c.1585C>T	NP_004620.1:p.Gln529Ter
ENST00000378643.7:c.1585C>T	ENSP00000367910.3:p.Gln529Ter
ENST00000425676.5:c.*1061C>T	ENSP00000412793.1:n.*1061C>T
ENST00000448890.2:c.1585C>T	ENSP00000409607.2:p.Gln529Ter
ENST00000461149.2:n.2973C>T
ENST00000476212.1:n.45-546C>T
ENST00000481254.1:n.393C>T
ENST00000696700.1:n.3008C>T
ENST00000696701.1:n.1885C>T
ENST00000696702.1:c.*1036C>T	ENSP00000512821.1:n.*1036C>T
ENST00000696703.1:c.*969C>T	ENSP00000512822.1:n.*969C>T
ENST00000696706.1:n.1648C>T
ENST00000696707.1:n.1802C>T
ENST00000696708.1:c.*930C>T	ENSP00000512825.1:n.*930C>T
ENST00000696709.1:n.2372C>T
ENST00000696710.1:c.1579C>T	ENSP00000512826.1:p.Gln527Ter
ENST00000696711.1:n.3840C>T
ENST00000696712.1:n.1872C>T
ENST00000696713.1:c.1585C>T	ENSP00000512827.1:p.Gln529Ter
ENST00000696714.1:n.2165C>T
ENST00000696715.1:c.1585C>T	ENSP00000512828.1:p.Gln529Ter