Canonical Allele Identifier: CA5039885

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076574C>T , CM000671.2:g.35076574C>T	GRCh38
NC_000009.11:g.35076571C>T , CM000671.1:g.35076571C>T	GRCh37
NC_000009.10:g.35066571C>T	NCBI36
NG_007312.1:g.8443G>A , LRG_499:g.8443G>A
NG_007887.1:g.1169G>A , LRG_657:g.1169G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.934G>A	ENSP00000409607.2:p.Val312Ile
ENST00000461149.2:n.2151G>A
ENST00000696700.1:n.2186G>A
ENST00000696701.1:n.1038G>A
ENST00000696702.1:c.*410G>A	ENSP00000512821.1:n.*410G>A
ENST00000696703.1:c.*410G>A	ENSP00000512822.1:n.*410G>A
ENST00000696706.1:n.997G>A
ENST00000696707.1:n.1151G>A
ENST00000696708.1:c.*279G>A	ENSP00000512825.1:n.*279G>A
ENST00000696709.1:n.1336G>A
ENST00000696710.1:c.934G>A	ENSP00000512826.1:p.Val312Ile
ENST00000696711.1:n.2383G>A
ENST00000696712.1:n.1050G>A
ENST00000696713.1:c.934G>A	ENSP00000512827.1:p.Val312Ile
ENST00000696714.1:n.1410G>A
ENST00000696715.1:c.934G>A	ENSP00000512828.1:p.Val312Ile
ENST00000378643.8:c.934G>A MANE Select	ENSP00000367910.4:p.Val312Ile
ENST00000378643.7:c.934G>A	ENSP00000367910.3:p.Val312Ile
ENST00000425676.5:c.*410G>A	ENSP00000412793.1:n.*410G>A
ENST00000474894.1:n.139G>A
NM_004629.1:c.934G>A , LRG_499t1:c.934G>A	NP_004620.1:p.Val312Ile
NM_004629.2:c.934G>A MANE Select	NP_004620.1:p.Val312Ile