Canonical Allele Identifier: CA373310024

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075976T>C , CM000671.2:g.35075976T>C	GRCh38
NC_000009.11:g.35075973T>C , CM000671.1:g.35075973T>C	GRCh37
NC_000009.10:g.35065973T>C	NCBI36
NG_007312.1:g.9041A>G , LRG_499:g.9041A>G
NG_007887.1:g.1767A>G , LRG_657:g.1767A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1129A>G MANE Select	NP_004620.1:p.Ser377Gly
ENST00000378643.8:c.1129A>G MANE Select	ENSP00000367910.4:p.Ser377Gly
NM_004629.1:c.1129A>G , LRG_499t1:c.1129A>G	NP_004620.1:p.Ser377Gly
ENST00000378643.7:c.1129A>G	ENSP00000367910.3:p.Ser377Gly
ENST00000425676.5:c.*605A>G	ENSP00000412793.1:n.*605A>G
ENST00000448890.2:c.1129A>G	ENSP00000409607.2:p.Ser377Gly
ENST00000461149.2:n.2346A>G
ENST00000476212.1:n.44+546A>G
ENST00000696700.1:n.2381A>G
ENST00000696701.1:n.1233A>G
ENST00000696702.1:c.*605A>G	ENSP00000512821.1:n.*605A>G
ENST00000696703.1:c.*553-247A>G	ENSP00000512822.1:n.*553-247A>G
ENST00000696706.1:n.1192A>G
ENST00000696707.1:n.1346A>G
ENST00000696708.1:c.*474A>G	ENSP00000512825.1:n.*474A>G
ENST00000696709.1:n.1513A>G
ENST00000696710.1:c.1129A>G	ENSP00000512826.1:p.Ser377Gly
ENST00000696711.1:n.2981A>G
ENST00000696712.1:n.1245A>G
ENST00000696713.1:c.1129A>G	ENSP00000512827.1:p.Ser377Gly
ENST00000696714.1:n.1553-247A>G
ENST00000696715.1:c.1129A>G	ENSP00000512828.1:p.Ser377Gly