Canonical Allele Identifier: CA373305096

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075066A>T , CM000671.2:g.35075066A>T	GRCh38
NC_000009.11:g.35075063A>T , CM000671.1:g.35075063A>T	GRCh37
NC_000009.10:g.35065063A>T	NCBI36
NG_007312.1:g.9951T>A , LRG_499:g.9951T>A
NG_007887.1:g.2677T>A , LRG_657:g.2677T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1497T>A MANE Select	NP_004620.1:p.Cys499Ter
ENST00000378643.8:c.1497T>A MANE Select	ENSP00000367910.4:p.Cys499Ter
NM_004629.1:c.1497T>A , LRG_499t1:c.1497T>A	NP_004620.1:p.Cys499Ter
ENST00000378643.7:c.1497T>A	ENSP00000367910.3:p.Cys499Ter
ENST00000425676.5:c.*973T>A	ENSP00000412793.1:n.*973T>A
ENST00000448890.2:c.1497T>A	ENSP00000409607.2:p.Cys499Ter
ENST00000461149.2:n.2885T>A
ENST00000476212.1:n.45-634T>A
ENST00000481254.1:n.305T>A
ENST00000696700.1:n.2920T>A
ENST00000696701.1:n.1797T>A
ENST00000696702.1:c.*948T>A	ENSP00000512821.1:n.*948T>A
ENST00000696703.1:c.*881T>A	ENSP00000512822.1:n.*881T>A
ENST00000696706.1:n.1560T>A
ENST00000696707.1:n.1714T>A
ENST00000696708.1:c.*842T>A	ENSP00000512825.1:n.*842T>A
ENST00000696709.1:n.2284T>A
ENST00000696710.1:c.1491T>A	ENSP00000512826.1:p.Cys497Ter
ENST00000696711.1:n.3752T>A
ENST00000696712.1:n.1784T>A
ENST00000696713.1:c.1497T>A	ENSP00000512827.1:p.Cys499Ter
ENST00000696714.1:n.2077T>A
ENST00000696715.1:c.1497T>A	ENSP00000512828.1:p.Cys499Ter