Canonical Allele Identifier: CA1139660966

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075706_35075716delinsG , CM000671.2:g.35075706_35075716delinsG	GRCh38
NC_000009.11:g.35075703_35075713delinsG , CM000671.1:g.35075703_35075713delinsG	GRCh37
NC_000009.10:g.35065703_35065713delinsG	NCBI36
NG_007312.1:g.9301_9311delinsC , LRG_499:g.9301_9311delinsC
NG_007887.1:g.2027_2037delinsC , LRG_657:g.2027_2037delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1182_1192delinsC	ENSP00000409607.2:p.Glu395TrpfsTer5
ENST00000461149.2:n.2374_2384delinsC
ENST00000696700.1:n.2409_2419delinsC
ENST00000696701.1:n.1286_1296delinsC
ENST00000696702.1:c.*633_*643delinsC	ENSP00000512821.1:n.*633_*643delinsC
ENST00000696703.1:c.*566_*576delinsC	ENSP00000512822.1:n.*566_*576delinsC
ENST00000696706.1:n.1245_1255delinsC
ENST00000696707.1:n.1399_1409delinsC
ENST00000696708.1:c.*527_*537delinsC	ENSP00000512825.1:n.*527_*537delinsC
ENST00000696709.1:n.1773_1783delinsC
ENST00000696710.1:c.1182_1192delinsC	ENSP00000512826.1:p.Glu395TrpfsTer5
ENST00000696711.1:n.3241_3251delinsC
ENST00000696712.1:n.1273_1283delinsC
ENST00000696713.1:c.1182_1192delinsC	ENSP00000512827.1:p.Glu395TrpfsTer5
ENST00000696714.1:n.1566_1576delinsC
ENST00000696715.1:c.1182_1192delinsC	ENSP00000512828.1:p.Glu395TrpfsTer5
ENST00000378643.8:c.1182_1192delinsC MANE Select	ENSP00000367910.4:p.Glu395TrpfsTer5
ENST00000378643.7:c.1182_1192delinsC	ENSP00000367910.3:p.Glu395TrpfsTer5
ENST00000425676.5:c.*658_*668delinsC	ENSP00000412793.1:n.*658_*668delinsC
ENST00000476212.1:n.44+806_44+816delinsC
NM_004629.1:c.1182_1192delinsC , LRG_499t1:c.1182_1192delinsC	NP_004620.1:p.Glu395TrpfsTer5
NM_004629.2:c.1182_1192delinsC MANE Select	NP_004620.1:p.Glu395TrpfsTer5