Canonical Allele Identifier: CA464602795

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075743G>A , CM000671.2:g.35075743G>A	GRCh38
NC_000009.11:g.35075740G>A , CM000671.1:g.35075740G>A	GRCh37
NC_000009.10:g.35065740G>A	NCBI36
NG_007312.1:g.9274C>T , LRG_499:g.9274C>T
NG_007887.1:g.2000C>T , LRG_657:g.2000C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1155C>T	ENSP00000409607.2:p.Pro385=
ENST00000461149.2:n.2361-14C>T
ENST00000696700.1:n.2396-14C>T
ENST00000696701.1:n.1259C>T
ENST00000696702.1:c.*620-14C>T	ENSP00000512821.1:n.*620-14C>T
ENST00000696703.1:c.*553-14C>T	ENSP00000512822.1:n.*553-14C>T
ENST00000696706.1:n.1218C>T
ENST00000696707.1:n.1372C>T
ENST00000696708.1:c.*500C>T	ENSP00000512825.1:n.*500C>T
ENST00000696709.1:n.1746C>T
ENST00000696710.1:c.1155C>T	ENSP00000512826.1:p.Pro385=
ENST00000696711.1:n.3214C>T
ENST00000696712.1:n.1260-14C>T
ENST00000696713.1:c.1155C>T	ENSP00000512827.1:p.Pro385=
ENST00000696714.1:n.1553-14C>T
ENST00000696715.1:c.1155C>T	ENSP00000512828.1:p.Pro385=
ENST00000378643.8:c.1155C>T MANE Select	ENSP00000367910.4:p.Pro385=
ENST00000378643.7:c.1155C>T	ENSP00000367910.3:p.Pro385=
ENST00000425676.5:c.*631C>T	ENSP00000412793.1:n.*631C>T
ENST00000476212.1:n.44+779C>T
NM_004629.1:c.1155C>T , LRG_499t1:c.1155C>T	NP_004620.1:p.Pro385=
NM_004629.2:c.1155C>T MANE Select	NP_004620.1:p.Pro385=