Canonical Allele Identifier: CA373301419

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074496T>C , CM000671.2:g.35074496T>C	GRCh38
NC_000009.11:g.35074493T>C , CM000671.1:g.35074493T>C	GRCh37
NC_000009.10:g.35064493T>C	NCBI36
NG_007312.1:g.10521A>G , LRG_499:g.10521A>G
NG_007887.1:g.3247A>G , LRG_657:g.3247A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1637-2A>G MANE Select	NP_004620.1:n.1637-2A>G
ENST00000378643.8:c.1637-2A>G MANE Select	ENSP00000367910.4:n.1637-2A>G
NM_004629.1:c.1637-2A>G , LRG_499t1:c.1637-2A>G	NP_004620.1:n.1637-2A>G
ENST00000378643.7:c.1637-2A>G	ENSP00000367910.3:n.1637-2A>G
ENST00000425676.5:c.*1113-2A>G	ENSP00000412793.1:n.*1113-2A>G
ENST00000448890.2:c.1637-2A>G	ENSP00000409607.2:n.1637-2A>G
ENST00000461149.2:n.3455A>G
ENST00000476212.1:n.45-64A>G
ENST00000696700.1:n.3490A>G
ENST00000696701.1:n.1937-2A>G
ENST00000696702.1:c.*1088-2A>G	ENSP00000512821.1:n.*1088-2A>G
ENST00000696703.1:c.*1021-2A>G	ENSP00000512822.1:n.*1021-2A>G
ENST00000696706.1:n.1700-2A>G
ENST00000696707.1:n.1854-2A>G
ENST00000696708.1:c.*982-2A>G	ENSP00000512825.1:n.*982-2A>G
ENST00000696709.1:n.2854A>G
ENST00000696710.1:c.1631-2A>G	ENSP00000512826.1:n.1631-2A>G
ENST00000696711.1:n.4322A>G
ENST00000696712.1:n.2354A>G
ENST00000696713.1:c.1637-34A>G	ENSP00000512827.1:n.1637-34A>G
ENST00000696714.1:n.2647A>G
ENST00000696715.1:c.1637-2A>G	ENSP00000512828.1:n.1637-2A>G