Canonical Allele Identifier: CA2689840767

Gene: FANCG

Linked Data

• gnomAD v4: 9-35076344-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076344C>G , CM000671.2:g.35076344C>G	GRCh38
NC_000009.11:g.35076341C>G , CM000671.1:g.35076341C>G	GRCh37
NC_000009.10:g.35066341C>G	NCBI36
NG_007312.1:g.8673G>C , LRG_499:g.8673G>C
NG_007887.1:g.1399G>C , LRG_657:g.1399G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000448890.2:c.1076+88G>C	ENSP00000409607.2:n.1076+88G>C
ENST00000461149.2:n.2293+88G>C
ENST00000696700.1:n.2328+88G>C
ENST00000696701.1:n.1180+88G>C
ENST00000696702.1:c.*552+88G>C	ENSP00000512821.1:n.*552+88G>C
ENST00000696703.1:c.*552+88G>C	ENSP00000512822.1:n.*552+88G>C
ENST00000696706.1:n.1139+88G>C
ENST00000696707.1:n.1293+88G>C
ENST00000696708.1:c.*421+88G>C	ENSP00000512825.1:n.*421+88G>C
ENST00000696709.1:n.1460+106G>C
ENST00000696710.1:c.1076+88G>C	ENSP00000512826.1:n.1076+88G>C
ENST00000696711.1:n.2613G>C
ENST00000696712.1:n.1192+88G>C
ENST00000696713.1:c.1076+88G>C	ENSP00000512827.1:n.1076+88G>C
ENST00000696714.1:n.1552+88G>C
ENST00000696715.1:c.1076+88G>C	ENSP00000512828.1:n.1076+88G>C
ENST00000378643.8:c.1076+88G>C MANE Select	ENSP00000367910.4:n.1076+88G>C
ENST00000378643.7:c.1076+88G>C	ENSP00000367910.3:n.1076+88G>C
ENST00000425676.5:c.*552+88G>C	ENSP00000412793.1:n.*552+88G>C
ENST00000474894.1:n.369G>C
ENST00000476212.1:n.44+178G>C
NM_004629.1:c.1076+88G>C , LRG_499t1:c.1076+88G>C	NP_004620.1:n.1076+88G>C
NM_004629.2:c.1076+88G>C MANE Select	NP_004620.1:n.1076+88G>C