Canonical Allele Identifier: CA192692677

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075285C>A , CM000671.2:g.35075285C>A	GRCh38
NC_000009.11:g.35075282C>A , CM000671.1:g.35075282C>A	GRCh37
NC_000009.10:g.35065282C>A	NCBI36
NG_007312.1:g.9732G>T , LRG_499:g.9732G>T
NG_007887.1:g.2458G>T , LRG_657:g.2458G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1474G>T MANE Select	NP_004620.1:p.Glu492Ter
ENST00000378643.8:c.1474G>T MANE Select	ENSP00000367910.4:p.Glu492Ter
NM_004629.1:c.1474G>T , LRG_499t1:c.1474G>T	NP_004620.1:p.Glu492Ter
ENST00000378643.7:c.1474G>T	ENSP00000367910.3:p.Glu492Ter
ENST00000425676.5:c.*950G>T	ENSP00000412793.1:n.*950G>T
ENST00000448890.2:c.1474G>T	ENSP00000409607.2:p.Glu492Ter
ENST00000461149.2:n.2666G>T
ENST00000476212.1:n.45-853G>T
ENST00000481254.1:n.86G>T
ENST00000696700.1:n.2701G>T
ENST00000696701.1:n.1578G>T
ENST00000696702.1:c.*925G>T	ENSP00000512821.1:n.*925G>T
ENST00000696703.1:c.*858G>T	ENSP00000512822.1:n.*858G>T
ENST00000696706.1:n.1537G>T
ENST00000696707.1:n.1691G>T
ENST00000696708.1:c.*819G>T	ENSP00000512825.1:n.*819G>T
ENST00000696709.1:n.2065G>T
ENST00000696710.1:c.1474G>T	ENSP00000512826.1:p.Glu492Ter
ENST00000696711.1:n.3533G>T
ENST00000696712.1:n.1565G>T
ENST00000696713.1:c.1474G>T	ENSP00000512827.1:p.Glu492Ter
ENST00000696714.1:n.1858G>T
ENST00000696715.1:c.1474G>T	ENSP00000512828.1:p.Glu492Ter