Canonical Allele Identifier: CA340607
Gene: FANCG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35074174_35074183del , CM000671.2:g.35074174_35074183del GRCh38
NC_000009.11:g.35074171_35074180del , CM000671.1:g.35074171_35074180del GRCh37
NC_000009.10:g.35064171_35064180del NCBI36
NG_007312.1:g.10835_10844del , LRG_499:g.10835_10844del
NG_007887.1:g.3561_3570del , LRG_657:g.3561_3570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000448890.2:c.1795_1804del ENSP00000409607.2:p.Trp599ProfsTer?
ENST00000461149.2:n.3769_3778del
ENST00000696700.1:n.3650_3659del
ENST00000696701.1:n.2095_2104del
ENST00000696702.1:c.*1246_*1255del ENSP00000512821.1:n.*1246_*1255del
ENST00000696703.1:c.*1179_*1188del ENSP00000512822.1:n.*1179_*1188del
ENST00000696706.1:n.1858_1867del
ENST00000696707.1:n.2012_2021del
ENST00000696708.1:c.*1140_*1149del ENSP00000512825.1:n.*1140_*1149del
ENST00000696709.1:n.3168_3177del
ENST00000696710.1:c.1789_1798del ENSP00000512826.1:p.Trp597ProfsTer?
ENST00000696711.1:n.4636_4645del
ENST00000696712.1:n.2514_2523del
ENST00000696713.1:c.*98_*107del ENSP00000512827.1:n.*98_*107del
ENST00000696714.1:n.2961_2970del
ENST00000696715.1:c.*185_*194del ENSP00000512828.1:n.*185_*194del
ENST00000378643.8:c.1795_1804del MANE Select ENSP00000367910.4:p.Trp599ProfsTer?
ENST00000378643.7:c.1795_1804del ENSP00000367910.3:p.Trp599ProfsTer?
ENST00000425676.5:c.*1271_*1280del ENSP00000412793.1:n.*1271_*1280del
ENST00000476212.1:n.141_150del
NM_004629.1:c.1795_1804del , LRG_499t1:c.1795_1804del NP_004620.1:p.Trp599ProfsTer?
NM_004629.2:c.1795_1804del MANE Select NP_004620.1:p.Trp599ProfsTer?
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