Canonical Allele Identifier: CA373312753

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076726C>A , CM000671.2:g.35076726C>A	GRCh38
NC_000009.11:g.35076723C>A , CM000671.1:g.35076723C>A	GRCh37
NC_000009.10:g.35066723C>A	NCBI36
NG_007312.1:g.8291G>T , LRG_499:g.8291G>T
NG_007887.1:g.1017G>T , LRG_657:g.1017G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.922G>T MANE Select	NP_004620.1:p.Glu308Ter
ENST00000378643.8:c.922G>T MANE Select	ENSP00000367910.4:p.Glu308Ter
NM_004629.1:c.922G>T , LRG_499t1:c.922G>T	NP_004620.1:p.Glu308Ter
ENST00000378643.7:c.922G>T	ENSP00000367910.3:p.Glu308Ter
ENST00000425676.5:c.*398G>T	ENSP00000412793.1:n.*398G>T
ENST00000448890.2:c.922G>T	ENSP00000409607.2:p.Glu308Ter
ENST00000461149.2:n.2139G>T
ENST00000474894.1:n.127G>T
ENST00000696700.1:n.2174G>T
ENST00000696701.1:n.1026G>T
ENST00000696702.1:c.*398G>T	ENSP00000512821.1:n.*398G>T
ENST00000696703.1:c.*398G>T	ENSP00000512822.1:n.*398G>T
ENST00000696706.1:n.985G>T
ENST00000696707.1:n.1139G>T
ENST00000696708.1:c.*267G>T	ENSP00000512825.1:n.*267G>T
ENST00000696709.1:n.1324G>T
ENST00000696710.1:c.922G>T	ENSP00000512826.1:p.Glu308Ter
ENST00000696711.1:n.2371G>T
ENST00000696712.1:n.1038G>T
ENST00000696713.1:c.922G>T	ENSP00000512827.1:p.Glu308Ter
ENST00000696714.1:n.1398G>T
ENST00000696715.1:c.922G>T	ENSP00000512828.1:p.Glu308Ter