Canonical Allele Identifier: CA5039731

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075286T>C , CM000671.2:g.35075286T>C	GRCh38
NC_000009.11:g.35075283T>C , CM000671.1:g.35075283T>C	GRCh37
NC_000009.10:g.35065283T>C	NCBI36
NG_007312.1:g.9731A>G , LRG_499:g.9731A>G
NG_007887.1:g.2457A>G , LRG_657:g.2457A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1473A>G MANE Select	NP_004620.1:p.Lys491=
ENST00000378643.8:c.1473A>G MANE Select	ENSP00000367910.4:p.Lys491=
NM_004629.1:c.1473A>G , LRG_499t1:c.1473A>G	NP_004620.1:p.Lys491=
ENST00000378643.7:c.1473A>G	ENSP00000367910.3:p.Lys491=
ENST00000425676.5:c.*949A>G	ENSP00000412793.1:n.*949A>G
ENST00000448890.2:c.1473A>G	ENSP00000409607.2:p.Lys491=
ENST00000461149.2:n.2665A>G
ENST00000476212.1:n.45-854A>G
ENST00000481254.1:n.85A>G
ENST00000696700.1:n.2700A>G
ENST00000696701.1:n.1577A>G
ENST00000696702.1:c.*924A>G	ENSP00000512821.1:n.*924A>G
ENST00000696703.1:c.*857A>G	ENSP00000512822.1:n.*857A>G
ENST00000696706.1:n.1536A>G
ENST00000696707.1:n.1690A>G
ENST00000696708.1:c.*818A>G	ENSP00000512825.1:n.*818A>G
ENST00000696709.1:n.2064A>G
ENST00000696710.1:c.1473A>G	ENSP00000512826.1:p.Lys491=
ENST00000696711.1:n.3532A>G
ENST00000696712.1:n.1564A>G
ENST00000696713.1:c.1473A>G	ENSP00000512827.1:p.Lys491=
ENST00000696714.1:n.1857A>G
ENST00000696715.1:c.1473A>G	ENSP00000512828.1:p.Lys491=