Canonical Allele Identifier: CA373304035

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074991C>T , CM000671.2:g.35074991C>T	GRCh38
NC_000009.11:g.35074988C>T , CM000671.1:g.35074988C>T	GRCh37
NC_000009.10:g.35064988C>T	NCBI36
NG_007312.1:g.10026G>A , LRG_499:g.10026G>A
NG_007887.1:g.2752G>A , LRG_657:g.2752G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1572G>A MANE Select	NP_004620.1:p.Trp524Ter
ENST00000378643.8:c.1572G>A MANE Select	ENSP00000367910.4:p.Trp524Ter
NM_004629.1:c.1572G>A , LRG_499t1:c.1572G>A	NP_004620.1:p.Trp524Ter
ENST00000378643.7:c.1572G>A	ENSP00000367910.3:p.Trp524Ter
ENST00000425676.5:c.*1048G>A	ENSP00000412793.1:n.*1048G>A
ENST00000448890.2:c.1572G>A	ENSP00000409607.2:p.Trp524Ter
ENST00000461149.2:n.2960G>A
ENST00000476212.1:n.45-559G>A
ENST00000481254.1:n.380G>A
ENST00000696700.1:n.2995G>A
ENST00000696701.1:n.1872G>A
ENST00000696702.1:c.*1023G>A	ENSP00000512821.1:n.*1023G>A
ENST00000696703.1:c.*956G>A	ENSP00000512822.1:n.*956G>A
ENST00000696706.1:n.1635G>A
ENST00000696707.1:n.1789G>A
ENST00000696708.1:c.*917G>A	ENSP00000512825.1:n.*917G>A
ENST00000696709.1:n.2359G>A
ENST00000696710.1:c.1566G>A	ENSP00000512826.1:p.Trp522Ter
ENST00000696711.1:n.3827G>A
ENST00000696712.1:n.1859G>A
ENST00000696713.1:c.1572G>A	ENSP00000512827.1:p.Trp524Ter
ENST00000696714.1:n.2152G>A
ENST00000696715.1:c.1572G>A	ENSP00000512828.1:p.Trp524Ter