Canonical Allele Identifier: CA1139660971

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076769dup , CM000671.2:g.35076769dup	GRCh38
NC_000009.11:g.35076766dup , CM000671.1:g.35076766dup	GRCh37
NC_000009.10:g.35066766dup	NCBI36
NG_007312.1:g.8252dup , LRG_499:g.8252dup
NG_007887.1:g.978dup , LRG_657:g.978dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.883dup	ENSP00000409607.2:p.Asp295GlyfsTer14
ENST00000461149.2:n.2100dup
ENST00000696700.1:n.2135dup
ENST00000696701.1:n.987dup
ENST00000696702.1:c.*359dup	ENSP00000512821.1:n.*359dup
ENST00000696703.1:c.*359dup	ENSP00000512822.1:n.*359dup
ENST00000696706.1:n.946dup
ENST00000696707.1:n.1100dup
ENST00000696708.1:c.*228dup	ENSP00000512825.1:n.*228dup
ENST00000696709.1:n.1285dup
ENST00000696710.1:c.883dup	ENSP00000512826.1:p.Asp295GlyfsTer14
ENST00000696711.1:n.2332dup
ENST00000696712.1:n.999dup
ENST00000696713.1:c.883dup	ENSP00000512827.1:p.Asp295GlyfsTer14
ENST00000696714.1:n.1359dup
ENST00000696715.1:c.883dup	ENSP00000512828.1:p.Asp295GlyfsTer14
ENST00000378643.8:c.883dup MANE Select	ENSP00000367910.4:p.Asp295GlyfsTer14
ENST00000378643.7:c.883dup	ENSP00000367910.3:p.Asp295GlyfsTer14
ENST00000425676.5:c.*359dup	ENSP00000412793.1:n.*359dup
ENST00000474894.1:n.88dup
NM_004629.1:c.883dup , LRG_499t1:c.883dup	NP_004620.1:p.Asp295GlyfsTer14
NM_004629.2:c.883dup MANE Select	NP_004620.1:p.Asp295GlyfsTer14