Canonical Allele Identifier: CA373303186

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074926C>T , CM000671.2:g.35074926C>T	GRCh38
NC_000009.11:g.35074923C>T , CM000671.1:g.35074923C>T	GRCh37
NC_000009.10:g.35064923C>T	NCBI36
NG_007312.1:g.10091G>A , LRG_499:g.10091G>A
NG_007887.1:g.2817G>A , LRG_657:g.2817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1636+1G>A	ENSP00000409607.2:n.1636+1G>A
ENST00000461149.2:n.3025G>A
ENST00000696700.1:n.3060G>A
ENST00000696701.1:n.1936+1G>A
ENST00000696702.1:c.*1087+1G>A	ENSP00000512821.1:n.*1087+1G>A
ENST00000696703.1:c.*1020+1G>A	ENSP00000512822.1:n.*1020+1G>A
ENST00000696706.1:n.1699+1G>A
ENST00000696707.1:n.1853+1G>A
ENST00000696708.1:c.*981+1G>A	ENSP00000512825.1:n.*981+1G>A
ENST00000696709.1:n.2424G>A
ENST00000696710.1:c.1630+1G>A	ENSP00000512826.1:n.1630+1G>A
ENST00000696711.1:n.3892G>A
ENST00000696712.1:n.1924G>A
ENST00000696713.1:c.1636+1G>A	ENSP00000512827.1:n.1636+1G>A
ENST00000696714.1:n.2217G>A
ENST00000696715.1:c.1636+1G>A	ENSP00000512828.1:n.1636+1G>A
ENST00000378643.8:c.1636+1G>A MANE Select	ENSP00000367910.4:n.1636+1G>A
ENST00000378643.7:c.1636+1G>A	ENSP00000367910.3:n.1636+1G>A
ENST00000425676.5:c.*1112+1G>A	ENSP00000412793.1:n.*1112+1G>A
ENST00000476212.1:n.45-494G>A
ENST00000481254.1:n.445G>A
NM_004629.1:c.1636+1G>A , LRG_499t1:c.1636+1G>A	NP_004620.1:n.1636+1G>A
NM_004629.2:c.1636+1G>A MANE Select	NP_004620.1:n.1636+1G>A