Canonical Allele Identifier: CA464413861

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075488T>C , CM000671.2:g.35075488T>C	GRCh38
NC_000009.11:g.35075485T>C , CM000671.1:g.35075485T>C	GRCh37
NC_000009.10:g.35065485T>C	NCBI36
NG_007312.1:g.9529A>G , LRG_499:g.9529A>G
NG_007887.1:g.2255A>G , LRG_657:g.2255A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1410A>G MANE Select	NP_004620.1:p.Lys470=
ENST00000378643.8:c.1410A>G MANE Select	ENSP00000367910.4:p.Lys470=
NM_004629.1:c.1410A>G , LRG_499t1:c.1410A>G	NP_004620.1:p.Lys470=
ENST00000378643.7:c.1410A>G	ENSP00000367910.3:p.Lys470=
ENST00000425676.5:c.*886A>G	ENSP00000412793.1:n.*886A>G
ENST00000448890.2:c.1410A>G	ENSP00000409607.2:p.Lys470=
ENST00000461149.2:n.2602A>G
ENST00000476212.1:n.44+1034A>G
ENST00000481254.1:n.22A>G
ENST00000696700.1:n.2637A>G
ENST00000696701.1:n.1514A>G
ENST00000696702.1:c.*861A>G	ENSP00000512821.1:n.*861A>G
ENST00000696703.1:c.*794A>G	ENSP00000512822.1:n.*794A>G
ENST00000696706.1:n.1473A>G
ENST00000696707.1:n.1627A>G
ENST00000696708.1:c.*755A>G	ENSP00000512825.1:n.*755A>G
ENST00000696709.1:n.2001A>G
ENST00000696710.1:c.1410A>G	ENSP00000512826.1:p.Lys470=
ENST00000696711.1:n.3469A>G
ENST00000696712.1:n.1501A>G
ENST00000696713.1:c.1410A>G	ENSP00000512827.1:p.Lys470=
ENST00000696714.1:n.1794A>G
ENST00000696715.1:c.1410A>G	ENSP00000512828.1:p.Lys470=