Canonical Allele Identifier: CA2838308545

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075401T>C , CM000671.2:g.35075401T>C	GRCh38
NC_000009.11:g.35075398T>C , CM000671.1:g.35075398T>C	GRCh37
NC_000009.10:g.35065398T>C	NCBI36
NG_007312.1:g.9616A>G , LRG_499:g.9616A>G
NG_007887.1:g.2342A>G , LRG_657:g.2342A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1433+64A>G	ENSP00000409607.2:n.1433+64A>G
ENST00000461149.2:n.2625+64A>G
ENST00000696700.1:n.2660+64A>G
ENST00000696701.1:n.1537+64A>G
ENST00000696702.1:c.*884+64A>G	ENSP00000512821.1:n.*884+64A>G
ENST00000696703.1:c.*817+64A>G	ENSP00000512822.1:n.*817+64A>G
ENST00000696706.1:n.1496+64A>G
ENST00000696707.1:n.1650+64A>G
ENST00000696708.1:c.*778+64A>G	ENSP00000512825.1:n.*778+64A>G
ENST00000696709.1:n.2024+64A>G
ENST00000696710.1:c.1433+64A>G	ENSP00000512826.1:n.1433+64A>G
ENST00000696711.1:n.3492+64A>G
ENST00000696712.1:n.1524+64A>G
ENST00000696713.1:c.1433+64A>G	ENSP00000512827.1:n.1433+64A>G
ENST00000696714.1:n.1817+64A>G
ENST00000696715.1:c.1433+64A>G	ENSP00000512828.1:n.1433+64A>G
ENST00000378643.8:c.1433+64A>G MANE Select	ENSP00000367910.4:n.1433+64A>G
ENST00000378643.7:c.1433+64A>G	ENSP00000367910.3:n.1433+64A>G
ENST00000425676.5:c.*909+64A>G	ENSP00000412793.1:n.*909+64A>G
ENST00000476212.1:n.45-969A>G
ENST00000481254.1:n.45+64A>G
NM_004629.1:c.1433+64A>G , LRG_499t1:c.1433+64A>G	NP_004620.1:n.1433+64A>G
NM_004629.2:c.1433+64A>G MANE Select	NP_004620.1:n.1433+64A>G