Canonical Allele Identifier: CA5039995

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35077252T>C , CM000671.2:g.35077252T>C	GRCh38
NC_000009.11:g.35077249T>C , CM000671.1:g.35077249T>C	GRCh37
NC_000009.10:g.35067249T>C	NCBI36
NG_007312.1:g.7765A>G , LRG_499:g.7765A>G
NG_007887.1:g.491A>G , LRG_657:g.491A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.646+12A>G	ENSP00000409607.2:n.646+12A>G
ENST00000461149.2:n.1863+12A>G
ENST00000696700.1:n.1898+12A>G
ENST00000696701.1:n.750+12A>G
ENST00000696702.1:c.*122+12A>G	ENSP00000512821.1:n.*122+12A>G
ENST00000696703.1:c.*122+12A>G	ENSP00000512822.1:n.*122+12A>G
ENST00000696706.1:n.709+12A>G
ENST00000696707.1:n.863+12A>G
ENST00000696708.1:c.*122+12A>G	ENSP00000512825.1:n.*122+12A>G
ENST00000696709.1:n.1048+12A>G
ENST00000696710.1:c.646+12A>G	ENSP00000512826.1:n.646+12A>G
ENST00000696711.1:n.1995+12A>G
ENST00000696712.1:n.733+12A>G
ENST00000696713.1:c.646+12A>G	ENSP00000512827.1:n.646+12A>G
ENST00000696714.1:n.1122+12A>G
ENST00000696715.1:c.646+12A>G	ENSP00000512828.1:n.646+12A>G
ENST00000378643.8:c.646+12A>G MANE Select	ENSP00000367910.4:n.646+12A>G
ENST00000378643.7:c.646+12A>G	ENSP00000367910.3:n.646+12A>G
ENST00000425676.5:c.*122+12A>G	ENSP00000412793.1:n.*122+12A>G
NM_004629.1:c.646+12A>G , LRG_499t1:c.646+12A>G	NP_004620.1:n.646+12A>G
NM_004629.2:c.646+12A>G MANE Select	NP_004620.1:n.646+12A>G