Canonical Allele Identifier: CA373315885

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35079449G>A , CM000671.2:g.35079449G>A	GRCh38
NC_000009.11:g.35079446G>A , CM000671.1:g.35079446G>A	GRCh37
NC_000009.10:g.35069446G>A	NCBI36
NG_007312.1:g.5568C>T , LRG_499:g.5568C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.76C>T MANE Select	NP_004620.1:p.Gln26Ter
ENST00000378643.8:c.76C>T MANE Select	ENSP00000367910.4:p.Gln26Ter
NM_004629.1:c.76C>T , LRG_499t1:c.76C>T	NP_004620.1:p.Gln26Ter
ENST00000378643.7:c.76C>T	ENSP00000367910.3:p.Gln26Ter
ENST00000425676.5:c.76C>T	ENSP00000412793.1:p.Gln26Ter
ENST00000448890.1:c.76C>T	ENSP00000409607.1:p.Gln26Ter
ENST00000448890.2:c.76C>T	ENSP00000409607.2:p.Gln26Ter
ENST00000461149.2:n.552C>T
ENST00000462124.1:n.221C>T
ENST00000696700.1:n.326C>T
ENST00000696701.1:n.291C>T
ENST00000696702.1:c.76C>T	ENSP00000512821.1:p.Gln26Ter
ENST00000696703.1:c.76C>T	ENSP00000512822.1:p.Gln26Ter
ENST00000696707.1:n.32C>T
ENST00000696708.1:c.76C>T	ENSP00000512825.1:p.Gln26Ter
ENST00000696709.1:n.478C>T
ENST00000696710.1:c.76C>T	ENSP00000512826.1:p.Gln26Ter
ENST00000696711.1:n.423C>T
ENST00000696713.1:c.76C>T	ENSP00000512827.1:p.Gln26Ter
ENST00000696714.1:n.556C>T
ENST00000696715.1:c.76C>T	ENSP00000512828.1:p.Gln26Ter