Canonical Allele Identifier: CA373303661

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074960G>A , CM000671.2:g.35074960G>A	GRCh38
NC_000009.11:g.35074957G>A , CM000671.1:g.35074957G>A	GRCh37
NC_000009.10:g.35064957G>A	NCBI36
NG_007312.1:g.10057C>T , LRG_499:g.10057C>T
NG_007887.1:g.2783C>T , LRG_657:g.2783C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1603C>T MANE Select	NP_004620.1:p.Gln535Ter
ENST00000378643.8:c.1603C>T MANE Select	ENSP00000367910.4:p.Gln535Ter
NM_004629.1:c.1603C>T , LRG_499t1:c.1603C>T	NP_004620.1:p.Gln535Ter
ENST00000378643.7:c.1603C>T	ENSP00000367910.3:p.Gln535Ter
ENST00000425676.5:c.*1079C>T	ENSP00000412793.1:n.*1079C>T
ENST00000448890.2:c.1603C>T	ENSP00000409607.2:p.Gln535Ter
ENST00000461149.2:n.2991C>T
ENST00000476212.1:n.45-528C>T
ENST00000481254.1:n.411C>T
ENST00000696700.1:n.3026C>T
ENST00000696701.1:n.1903C>T
ENST00000696702.1:c.*1054C>T	ENSP00000512821.1:n.*1054C>T
ENST00000696703.1:c.*987C>T	ENSP00000512822.1:n.*987C>T
ENST00000696706.1:n.1666C>T
ENST00000696707.1:n.1820C>T
ENST00000696708.1:c.*948C>T	ENSP00000512825.1:n.*948C>T
ENST00000696709.1:n.2390C>T
ENST00000696710.1:c.1597C>T	ENSP00000512826.1:p.Gln533Ter
ENST00000696711.1:n.3858C>T
ENST00000696712.1:n.1890C>T
ENST00000696713.1:c.1603C>T	ENSP00000512827.1:p.Gln535Ter
ENST00000696714.1:n.2183C>T
ENST00000696715.1:c.1603C>T	ENSP00000512828.1:p.Gln535Ter