Canonical Allele Identifier: CA464602891

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35078620G>T , CM000671.2:g.35078620G>T	GRCh38
NC_000009.11:g.35078617G>T , CM000671.1:g.35078617G>T	GRCh37
NC_000009.10:g.35068617G>T	NCBI36
NG_007312.1:g.6397C>A , LRG_499:g.6397C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.292C>A MANE Select	NP_004620.1:p.Arg98=
ENST00000378643.8:c.292C>A MANE Select	ENSP00000367910.4:p.Arg98=
NM_004629.1:c.292C>A , LRG_499t1:c.292C>A	NP_004620.1:p.Arg98=
ENST00000378643.7:c.292C>A	ENSP00000367910.3:p.Arg98=
ENST00000425676.5:c.292C>A	ENSP00000412793.1:p.Arg98=
ENST00000448890.1:c.292C>A	ENSP00000409607.1:p.Arg98=
ENST00000448890.2:c.292C>A	ENSP00000409607.2:p.Arg98=
ENST00000461149.1:n.27C>A
ENST00000461149.2:n.768C>A
ENST00000462124.1:n.636C>A
ENST00000696700.1:n.542C>A
ENST00000696701.1:n.507C>A
ENST00000696702.1:c.292C>A	ENSP00000512821.1:p.Arg98=
ENST00000696703.1:c.292C>A	ENSP00000512822.1:p.Arg98=
ENST00000696706.1:n.355C>A
ENST00000696707.1:n.248C>A
ENST00000696708.1:c.292C>A	ENSP00000512825.1:p.Arg98=
ENST00000696709.1:n.694C>A
ENST00000696710.1:c.292C>A	ENSP00000512826.1:p.Arg98=
ENST00000696711.1:n.639C>A
ENST00000696713.1:c.292C>A	ENSP00000512827.1:p.Arg98=
ENST00000696714.1:n.971C>A
ENST00000696715.1:c.292C>A	ENSP00000512828.1:p.Arg98=