Canonical Allele Identifier: CA373300665

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074416C>T , CM000671.2:g.35074416C>T	GRCh38
NC_000009.11:g.35074413C>T , CM000671.1:g.35074413C>T	GRCh37
NC_000009.10:g.35064413C>T	NCBI36
NG_007312.1:g.10601G>A , LRG_499:g.10601G>A
NG_007887.1:g.3327G>A , LRG_657:g.3327G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1715G>A	ENSP00000409607.2:p.Trp572Ter
ENST00000461149.2:n.3535G>A
ENST00000696700.1:n.3570G>A
ENST00000696701.1:n.2015G>A
ENST00000696702.1:c.*1166G>A	ENSP00000512821.1:n.*1166G>A
ENST00000696703.1:c.*1099G>A	ENSP00000512822.1:n.*1099G>A
ENST00000696706.1:n.1778G>A
ENST00000696707.1:n.1932G>A
ENST00000696708.1:c.*1060G>A	ENSP00000512825.1:n.*1060G>A
ENST00000696709.1:n.2934G>A
ENST00000696710.1:c.1709G>A	ENSP00000512826.1:p.Trp570Ter
ENST00000696711.1:n.4402G>A
ENST00000696712.1:n.2434G>A
ENST00000696713.1:c.*18G>A	ENSP00000512827.1:n.*18G>A
ENST00000696714.1:n.2727G>A
ENST00000696715.1:c.1715G>A	ENSP00000512828.1:p.Trp572Ter
ENST00000378643.8:c.1715G>A MANE Select	ENSP00000367910.4:p.Trp572Ter
ENST00000378643.7:c.1715G>A	ENSP00000367910.3:p.Trp572Ter
ENST00000425676.5:c.*1191G>A	ENSP00000412793.1:n.*1191G>A
ENST00000476212.1:n.61G>A
NM_004629.1:c.1715G>A , LRG_499t1:c.1715G>A	NP_004620.1:p.Trp572Ter
NM_004629.2:c.1715G>A MANE Select	NP_004620.1:p.Trp572Ter