Canonical Allele Identifier: CA373314586

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35078305G>A , CM000671.2:g.35078305G>A	GRCh38
NC_000009.11:g.35078302G>A , CM000671.1:g.35078302G>A	GRCh37
NC_000009.10:g.35068302G>A	NCBI36
NG_007312.1:g.6712C>T , LRG_499:g.6712C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.346C>T MANE Select	NP_004620.1:p.Gln116Ter
ENST00000378643.8:c.346C>T MANE Select	ENSP00000367910.4:p.Gln116Ter
NM_004629.1:c.346C>T , LRG_499t1:c.346C>T	NP_004620.1:p.Gln116Ter
ENST00000378643.7:c.346C>T	ENSP00000367910.3:p.Gln116Ter
ENST00000425676.5:c.307+300C>T	ENSP00000412793.1:n.307+300C>T
ENST00000448890.1:c.346C>T	ENSP00000409607.1:p.Gln116Ter
ENST00000448890.2:c.346C>T	ENSP00000409607.2:p.Gln116Ter
ENST00000461149.1:n.81C>T
ENST00000461149.2:n.822C>T
ENST00000696700.1:n.857C>T
ENST00000696701.1:n.523-228C>T
ENST00000696702.1:c.307+300C>T	ENSP00000512821.1:n.307+300C>T
ENST00000696703.1:c.307+300C>T	ENSP00000512822.1:n.307+300C>T
ENST00000696706.1:n.409C>T
ENST00000696707.1:n.563C>T
ENST00000696708.1:c.307+300C>T	ENSP00000512825.1:n.307+300C>T
ENST00000696709.1:n.748C>T
ENST00000696710.1:c.346C>T	ENSP00000512826.1:p.Gln116Ter
ENST00000696711.1:n.954C>T
ENST00000696713.1:c.346C>T	ENSP00000512827.1:p.Gln116Ter
ENST00000696714.1:n.986+300C>T
ENST00000696715.1:c.346C>T	ENSP00000512828.1:p.Gln116Ter