Canonical Allele Identifier: CA5039612

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074164G>A , CM000671.2:g.35074164G>A	GRCh38
NC_000009.11:g.35074161G>A , CM000671.1:g.35074161G>A	GRCh37
NC_000009.10:g.35064161G>A	NCBI36
NG_007312.1:g.10853C>T , LRG_499:g.10853C>T
NG_007887.1:g.3579C>T , LRG_657:g.3579C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1813C>T	ENSP00000409607.2:p.Arg605Cys
ENST00000461149.2:n.3787C>T
ENST00000696700.1:n.3668C>T
ENST00000696701.1:n.2113C>T
ENST00000696702.1:c.*1264C>T	ENSP00000512821.1:n.*1264C>T
ENST00000696703.1:c.*1197C>T	ENSP00000512822.1:n.*1197C>T
ENST00000696706.1:n.1876C>T
ENST00000696707.1:n.2030C>T
ENST00000696708.1:c.*1158C>T	ENSP00000512825.1:n.*1158C>T
ENST00000696709.1:n.3186C>T
ENST00000696710.1:c.1807C>T	ENSP00000512826.1:p.Arg603Cys
ENST00000696711.1:n.4654C>T
ENST00000696712.1:n.2532C>T
ENST00000696713.1:c.*116C>T	ENSP00000512827.1:n.*116C>T
ENST00000696714.1:n.2979C>T
ENST00000696715.1:c.*203C>T	ENSP00000512828.1:n.*203C>T
ENST00000378643.8:c.1813C>T MANE Select	ENSP00000367910.4:p.Arg605Cys
ENST00000681845.1:c.12C>T
ENST00000378643.7:c.1813C>T	ENSP00000367910.3:p.Arg605Cys
ENST00000425676.5:c.*1289C>T	ENSP00000412793.1:n.*1289C>T
ENST00000476212.1:n.159C>T
NM_004629.1:c.1813C>T , LRG_499t1:c.1813C>T	NP_004620.1:p.Arg605Cys
NM_004629.2:c.1813C>T MANE Select	NP_004620.1:p.Arg605Cys