Canonical Allele Identifier: CA5039880

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076551C>G , CM000671.2:g.35076551C>G	GRCh38
NC_000009.11:g.35076548C>G , CM000671.1:g.35076548C>G	GRCh37
NC_000009.10:g.35066548C>G	NCBI36
NG_007312.1:g.8466G>C , LRG_499:g.8466G>C
NG_007887.1:g.1192G>C , LRG_657:g.1192G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.957G>C	ENSP00000409607.2:p.Pro319=
ENST00000461149.2:n.2174G>C
ENST00000696700.1:n.2209G>C
ENST00000696701.1:n.1061G>C
ENST00000696702.1:c.*433G>C	ENSP00000512821.1:n.*433G>C
ENST00000696703.1:c.*433G>C	ENSP00000512822.1:n.*433G>C
ENST00000696706.1:n.1020G>C
ENST00000696707.1:n.1174G>C
ENST00000696708.1:c.*302G>C	ENSP00000512825.1:n.*302G>C
ENST00000696709.1:n.1359G>C
ENST00000696710.1:c.957G>C	ENSP00000512826.1:p.Pro319=
ENST00000696711.1:n.2406G>C
ENST00000696712.1:n.1073G>C
ENST00000696713.1:c.957G>C	ENSP00000512827.1:p.Pro319=
ENST00000696714.1:n.1433G>C
ENST00000696715.1:c.957G>C	ENSP00000512828.1:p.Pro319=
ENST00000378643.8:c.957G>C MANE Select	ENSP00000367910.4:p.Pro319=
ENST00000378643.7:c.957G>C	ENSP00000367910.3:p.Pro319=
ENST00000425676.5:c.*433G>C	ENSP00000412793.1:n.*433G>C
ENST00000474894.1:n.162G>C
ENST00000476212.1:n.15G>C
NM_004629.1:c.957G>C , LRG_499t1:c.957G>C	NP_004620.1:p.Pro319=
NM_004629.2:c.957G>C MANE Select	NP_004620.1:p.Pro319=