Canonical Allele Identifier: CA5039656

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074469C>T , CM000671.2:g.35074469C>T	GRCh38
NC_000009.11:g.35074466C>T , CM000671.1:g.35074466C>T	GRCh37
NC_000009.10:g.35064466C>T	NCBI36
NG_007312.1:g.10548G>A , LRG_499:g.10548G>A
NG_007887.1:g.3274G>A , LRG_657:g.3274G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1662G>A MANE Select	NP_004620.1:p.Leu554=
ENST00000378643.8:c.1662G>A MANE Select	ENSP00000367910.4:p.Leu554=
NM_004629.1:c.1662G>A , LRG_499t1:c.1662G>A	NP_004620.1:p.Leu554=
ENST00000378643.7:c.1662G>A	ENSP00000367910.3:p.Leu554=
ENST00000425676.5:c.*1138G>A	ENSP00000412793.1:n.*1138G>A
ENST00000448890.2:c.1662G>A	ENSP00000409607.2:p.Leu554=
ENST00000461149.2:n.3482G>A
ENST00000476212.1:n.45-37G>A
ENST00000696700.1:n.3517G>A
ENST00000696701.1:n.1962G>A
ENST00000696702.1:c.*1113G>A	ENSP00000512821.1:n.*1113G>A
ENST00000696703.1:c.*1046G>A	ENSP00000512822.1:n.*1046G>A
ENST00000696706.1:n.1725G>A
ENST00000696707.1:n.1879G>A
ENST00000696708.1:c.*1007G>A	ENSP00000512825.1:n.*1007G>A
ENST00000696709.1:n.2881G>A
ENST00000696710.1:c.1656G>A	ENSP00000512826.1:p.Leu552=
ENST00000696711.1:n.4349G>A
ENST00000696712.1:n.2381G>A
ENST00000696713.1:c.1637-7G>A	ENSP00000512827.1:n.1637-7G>A
ENST00000696714.1:n.2674G>A
ENST00000696715.1:c.1662G>A	ENSP00000512828.1:p.Leu554=