Canonical Allele Identifier: CA373300432

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074386T>C , CM000671.2:g.35074386T>C	GRCh38
NC_000009.11:g.35074383T>C , CM000671.1:g.35074383T>C	GRCh37
NC_000009.10:g.35064383T>C	NCBI36
NG_007312.1:g.10631A>G , LRG_499:g.10631A>G
NG_007887.1:g.3357A>G , LRG_657:g.3357A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1745A>G	ENSP00000409607.2:p.His582Arg
ENST00000461149.2:n.3565A>G
ENST00000696700.1:n.3600A>G
ENST00000696701.1:n.2045A>G
ENST00000696702.1:c.*1196A>G	ENSP00000512821.1:n.*1196A>G
ENST00000696703.1:c.*1129A>G	ENSP00000512822.1:n.*1129A>G
ENST00000696706.1:n.1808A>G
ENST00000696707.1:n.1962A>G
ENST00000696708.1:c.*1090A>G	ENSP00000512825.1:n.*1090A>G
ENST00000696709.1:n.2964A>G
ENST00000696710.1:c.1739A>G	ENSP00000512826.1:p.His580Arg
ENST00000696711.1:n.4432A>G
ENST00000696712.1:n.2464A>G
ENST00000696713.1:c.*48A>G	ENSP00000512827.1:n.*48A>G
ENST00000696714.1:n.2757A>G
ENST00000696715.1:c.1745A>G	ENSP00000512828.1:p.His582Arg
ENST00000378643.8:c.1745A>G MANE Select	ENSP00000367910.4:p.His582Arg
ENST00000378643.7:c.1745A>G	ENSP00000367910.3:p.His582Arg
ENST00000425676.5:c.*1221A>G	ENSP00000412793.1:n.*1221A>G
ENST00000476212.1:n.91A>G
NM_004629.1:c.1745A>G , LRG_499t1:c.1745A>G	NP_004620.1:p.His582Arg
NM_004629.2:c.1745A>G MANE Select	NP_004620.1:p.His582Arg