Canonical Allele Identifier: CA373310348

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076023C>T , CM000671.2:g.35076023C>T	GRCh38
NC_000009.11:g.35076020C>T , CM000671.1:g.35076020C>T	GRCh37
NC_000009.10:g.35066020C>T	NCBI36
NG_007312.1:g.8994G>A , LRG_499:g.8994G>A
NG_007887.1:g.1720G>A , LRG_657:g.1720G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1082G>A MANE Select	NP_004620.1:p.Gly361Glu
ENST00000378643.8:c.1082G>A MANE Select	ENSP00000367910.4:p.Gly361Glu
NM_004629.1:c.1082G>A , LRG_499t1:c.1082G>A	NP_004620.1:p.Gly361Glu
ENST00000378643.7:c.1082G>A	ENSP00000367910.3:p.Gly361Glu
ENST00000425676.5:c.*558G>A	ENSP00000412793.1:n.*558G>A
ENST00000448890.2:c.1082G>A	ENSP00000409607.2:p.Gly361Glu
ENST00000461149.2:n.2299G>A
ENST00000476212.1:n.44+499G>A
ENST00000696700.1:n.2334G>A
ENST00000696701.1:n.1186G>A
ENST00000696702.1:c.*558G>A	ENSP00000512821.1:n.*558G>A
ENST00000696703.1:c.*553-294G>A	ENSP00000512822.1:n.*553-294G>A
ENST00000696706.1:n.1145G>A
ENST00000696707.1:n.1299G>A
ENST00000696708.1:c.*427G>A	ENSP00000512825.1:n.*427G>A
ENST00000696709.1:n.1466G>A
ENST00000696710.1:c.1082G>A	ENSP00000512826.1:p.Gly361Glu
ENST00000696711.1:n.2934G>A
ENST00000696712.1:n.1198G>A
ENST00000696713.1:c.1082G>A	ENSP00000512827.1:p.Gly361Glu
ENST00000696714.1:n.1553-294G>A
ENST00000696715.1:c.1082G>A	ENSP00000512828.1:p.Gly361Glu