Canonical Allele Identifier: CA1845839762

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076442G= , CM000671.2:g.35076442G=	GRCh38
NC_000009.11:g.35076439G= , CM000671.1:g.35076439G=	GRCh37
NC_000009.10:g.35066439G=	NCBI36
NG_007312.1:g.8575C= , LRG_499:g.8575C=
NG_007887.1:g.1301C= , LRG_657:g.1301C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1066C= MANE Select	NP_004620.1:p.Gln356=
ENST00000378643.8:c.1066C= MANE Select	ENSP00000367910.4:p.Gln356=
NM_004629.1:c.1066C= , LRG_499t1:c.1066C=	NP_004620.1:p.Gln356=
ENST00000378643.7:c.1066C=	ENSP00000367910.3:p.Gln356=
ENST00000425676.5:c.*542C=	ENSP00000412793.1:n.*542C=
ENST00000448890.2:c.1066C=	ENSP00000409607.2:p.Gln356=
ENST00000461149.2:n.2283C=
ENST00000474894.1:n.271C=
ENST00000476212.1:n.44+80C=
ENST00000696700.1:n.2318C=
ENST00000696701.1:n.1170C=
ENST00000696702.1:c.*542C=	ENSP00000512821.1:n.*542C=
ENST00000696703.1:c.*542C=	ENSP00000512822.1:n.*542C=
ENST00000696706.1:n.1129C=
ENST00000696707.1:n.1283C=
ENST00000696708.1:c.*411C=	ENSP00000512825.1:n.*411C=
ENST00000696709.1:n.1460+8C=
ENST00000696710.1:c.1066C=	ENSP00000512826.1:p.Gln356=
ENST00000696711.1:n.2515C=
ENST00000696712.1:n.1182C=
ENST00000696713.1:c.1066C=	ENSP00000512827.1:p.Gln356=
ENST00000696714.1:n.1542C=
ENST00000696715.1:c.1066C=	ENSP00000512828.1:p.Gln356=