Canonical Allele Identifier: CA373313084

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35076812C>T , CM000671.2:g.35076812C>T	GRCh38
NC_000009.11:g.35076809C>T , CM000671.1:g.35076809C>T	GRCh37
NC_000009.10:g.35066809C>T	NCBI36
NG_007312.1:g.8205G>A , LRG_499:g.8205G>A
NG_007887.1:g.931G>A , LRG_657:g.931G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.836G>A MANE Select	NP_004620.1:p.Trp279Ter
ENST00000378643.8:c.836G>A MANE Select	ENSP00000367910.4:p.Trp279Ter
NM_004629.1:c.836G>A , LRG_499t1:c.836G>A	NP_004620.1:p.Trp279Ter
ENST00000378643.7:c.836G>A	ENSP00000367910.3:p.Trp279Ter
ENST00000425676.5:c.*312G>A	ENSP00000412793.1:n.*312G>A
ENST00000448890.2:c.836G>A	ENSP00000409607.2:p.Trp279Ter
ENST00000461149.2:n.2053G>A
ENST00000474894.1:n.41G>A
ENST00000696700.1:n.2088G>A
ENST00000696701.1:n.940G>A
ENST00000696702.1:c.*312G>A	ENSP00000512821.1:n.*312G>A
ENST00000696703.1:c.*312G>A	ENSP00000512822.1:n.*312G>A
ENST00000696706.1:n.899G>A
ENST00000696707.1:n.1053G>A
ENST00000696708.1:c.*181G>A	ENSP00000512825.1:n.*181G>A
ENST00000696709.1:n.1238G>A
ENST00000696710.1:c.836G>A	ENSP00000512826.1:p.Trp279Ter
ENST00000696711.1:n.2285G>A
ENST00000696712.1:n.952G>A
ENST00000696713.1:c.836G>A	ENSP00000512827.1:p.Trp279Ter
ENST00000696714.1:n.1312G>A
ENST00000696715.1:c.836G>A	ENSP00000512828.1:p.Trp279Ter