Canonical Allele Identifier: CA5039626

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074218T>G , CM000671.2:g.35074218T>G	GRCh38
NC_000009.11:g.35074215T>G , CM000671.1:g.35074215T>G	GRCh37
NC_000009.10:g.35064215T>G	NCBI36
NG_007312.1:g.10799A>C , LRG_499:g.10799A>C
NG_007887.1:g.3525A>C , LRG_657:g.3525A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1761-2A>C	ENSP00000409607.2:n.1761-2A>C
ENST00000461149.2:n.3733A>C
ENST00000696700.1:n.3616-2A>C
ENST00000696701.1:n.2061-2A>C
ENST00000696702.1:c.*1212-2A>C	ENSP00000512821.1:n.*1212-2A>C
ENST00000696703.1:c.*1145-2A>C	ENSP00000512822.1:n.*1145-2A>C
ENST00000696706.1:n.1824-2A>C
ENST00000696707.1:n.1978-2A>C
ENST00000696708.1:c.*1106-2A>C	ENSP00000512825.1:n.*1106-2A>C
ENST00000696709.1:n.3132A>C
ENST00000696710.1:c.1755-2A>C	ENSP00000512826.1:n.1755-2A>C
ENST00000696711.1:n.4600A>C
ENST00000696712.1:n.2480-2A>C
ENST00000696713.1:c.*64-2A>C	ENSP00000512827.1:n.*64-2A>C
ENST00000696714.1:n.2925A>C
ENST00000696715.1:c.*149A>C	ENSP00000512828.1:n.*149A>C
ENST00000378643.8:c.1761-2A>C MANE Select	ENSP00000367910.4:n.1761-2A>C
ENST00000378643.7:c.1761-2A>C	ENSP00000367910.3:n.1761-2A>C
ENST00000425676.5:c.*1237-2A>C	ENSP00000412793.1:n.*1237-2A>C
ENST00000476212.1:n.107-2A>C
NM_004629.1:c.1761-2A>C , LRG_499t1:c.1761-2A>C	NP_004620.1:n.1761-2A>C
NM_004629.2:c.1761-2A>C MANE Select	NP_004620.1:n.1761-2A>C