Canonical Allele Identifier: CA1139660970

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076749del , CM000671.2:g.35076749del	GRCh38
NC_000009.11:g.35076746del , CM000671.1:g.35076746del	GRCh37
NC_000009.10:g.35066746del	NCBI36
NG_007312.1:g.8268del , LRG_499:g.8268del
NG_007887.1:g.994del , LRG_657:g.994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.899del	ENSP00000409607.2:p.Leu300ArgfsTer7
ENST00000461149.2:n.2116del
ENST00000696700.1:n.2151del
ENST00000696701.1:n.1003del
ENST00000696702.1:c.*375del	ENSP00000512821.1:n.*375del
ENST00000696703.1:c.*375del	ENSP00000512822.1:n.*375del
ENST00000696706.1:n.962del
ENST00000696707.1:n.1116del
ENST00000696708.1:c.*244del	ENSP00000512825.1:n.*244del
ENST00000696709.1:n.1301del
ENST00000696710.1:c.899del	ENSP00000512826.1:p.Leu300ArgfsTer7
ENST00000696711.1:n.2348del
ENST00000696712.1:n.1015del
ENST00000696713.1:c.899del	ENSP00000512827.1:p.Leu300ArgfsTer7
ENST00000696714.1:n.1375del
ENST00000696715.1:c.899del	ENSP00000512828.1:p.Leu300ArgfsTer7
ENST00000378643.8:c.899del MANE Select	ENSP00000367910.4:p.Leu300ArgfsTer7
ENST00000378643.7:c.899del	ENSP00000367910.3:p.Leu300ArgfsTer7
ENST00000425676.5:c.*375del	ENSP00000412793.1:n.*375del
ENST00000474894.1:n.104del
NM_004629.1:c.899del , LRG_499t1:c.899del	NP_004620.1:p.Leu300ArgfsTer7
NM_004629.2:c.899del MANE Select	NP_004620.1:p.Leu300ArgfsTer7