Canonical Allele Identifier: CA373306406

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075464C>T , CM000671.2:g.35075464C>T	GRCh38
NC_000009.11:g.35075461C>T , CM000671.1:g.35075461C>T	GRCh37
NC_000009.10:g.35065461C>T	NCBI36
NG_007312.1:g.9553G>A , LRG_499:g.9553G>A
NG_007887.1:g.2279G>A , LRG_657:g.2279G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1433+1G>A MANE Select	NP_004620.1:n.1433+1G>A
ENST00000378643.8:c.1433+1G>A MANE Select	ENSP00000367910.4:n.1433+1G>A
NM_004629.1:c.1433+1G>A , LRG_499t1:c.1433+1G>A	NP_004620.1:n.1433+1G>A
ENST00000378643.7:c.1433+1G>A	ENSP00000367910.3:n.1433+1G>A
ENST00000425676.5:c.*909+1G>A	ENSP00000412793.1:n.*909+1G>A
ENST00000448890.2:c.1433+1G>A	ENSP00000409607.2:n.1433+1G>A
ENST00000461149.2:n.2625+1G>A
ENST00000476212.1:n.45-1032G>A
ENST00000481254.1:n.45+1G>A
ENST00000696700.1:n.2660+1G>A
ENST00000696701.1:n.1537+1G>A
ENST00000696702.1:c.*884+1G>A	ENSP00000512821.1:n.*884+1G>A
ENST00000696703.1:c.*817+1G>A	ENSP00000512822.1:n.*817+1G>A
ENST00000696706.1:n.1496+1G>A
ENST00000696707.1:n.1650+1G>A
ENST00000696708.1:c.*778+1G>A	ENSP00000512825.1:n.*778+1G>A
ENST00000696709.1:n.2024+1G>A
ENST00000696710.1:c.1433+1G>A	ENSP00000512826.1:n.1433+1G>A
ENST00000696711.1:n.3492+1G>A
ENST00000696712.1:n.1524+1G>A
ENST00000696713.1:c.1433+1G>A	ENSP00000512827.1:n.1433+1G>A
ENST00000696714.1:n.1817+1G>A
ENST00000696715.1:c.1433+1G>A	ENSP00000512828.1:n.1433+1G>A