Canonical Allele Identifier: CA5040162

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35079470T>C , CM000671.2:g.35079470T>C	GRCh38
NC_000009.11:g.35079467T>C , CM000671.1:g.35079467T>C	GRCh37
NC_000009.10:g.35069467T>C	NCBI36
NG_007312.1:g.5547A>G , LRG_499:g.5547A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.55A>G MANE Select	NP_004620.1:p.Lys19Glu
ENST00000378643.8:c.55A>G MANE Select	ENSP00000367910.4:p.Lys19Glu
NM_004629.1:c.55A>G , LRG_499t1:c.55A>G	NP_004620.1:p.Lys19Glu
ENST00000378643.7:c.55A>G	ENSP00000367910.3:p.Lys19Glu
ENST00000425676.5:c.55A>G	ENSP00000412793.1:p.Lys19Glu
ENST00000448890.1:c.55A>G	ENSP00000409607.1:p.Lys19Glu
ENST00000448890.2:c.55A>G	ENSP00000409607.2:p.Lys19Glu
ENST00000461149.2:n.531A>G
ENST00000462124.1:n.200A>G
ENST00000696700.1:n.305A>G
ENST00000696701.1:n.270A>G
ENST00000696702.1:c.55A>G	ENSP00000512821.1:p.Lys19Glu
ENST00000696703.1:c.55A>G	ENSP00000512822.1:p.Lys19Glu
ENST00000696707.1:n.11A>G
ENST00000696708.1:c.55A>G	ENSP00000512825.1:p.Lys19Glu
ENST00000696709.1:n.457A>G
ENST00000696710.1:c.55A>G	ENSP00000512826.1:p.Lys19Glu
ENST00000696711.1:n.402A>G
ENST00000696713.1:c.55A>G	ENSP00000512827.1:p.Lys19Glu
ENST00000696714.1:n.535A>G
ENST00000696715.1:c.55A>G	ENSP00000512828.1:p.Lys19Glu