Canonical Allele Identifier: CA373309779

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075755C>T , CM000671.2:g.35075755C>T	GRCh38
NC_000009.11:g.35075752C>T , CM000671.1:g.35075752C>T	GRCh37
NC_000009.10:g.35065752C>T	NCBI36
NG_007312.1:g.9262G>A , LRG_499:g.9262G>A
NG_007887.1:g.1988G>A , LRG_657:g.1988G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1144-1G>A MANE Select	NP_004620.1:n.1144-1G>A
ENST00000378643.8:c.1144-1G>A MANE Select	ENSP00000367910.4:n.1144-1G>A
NM_004629.1:c.1144-1G>A , LRG_499t1:c.1144-1G>A	NP_004620.1:n.1144-1G>A
ENST00000378643.7:c.1144-1G>A	ENSP00000367910.3:n.1144-1G>A
ENST00000425676.5:c.*620-1G>A	ENSP00000412793.1:n.*620-1G>A
ENST00000448890.2:c.1144-1G>A	ENSP00000409607.2:n.1144-1G>A
ENST00000461149.2:n.2361-26G>A
ENST00000476212.1:n.44+767G>A
ENST00000696700.1:n.2396-26G>A
ENST00000696701.1:n.1248-1G>A
ENST00000696702.1:c.*620-26G>A	ENSP00000512821.1:n.*620-26G>A
ENST00000696703.1:c.*553-26G>A	ENSP00000512822.1:n.*553-26G>A
ENST00000696706.1:n.1207-1G>A
ENST00000696707.1:n.1361-1G>A
ENST00000696708.1:c.*489-1G>A	ENSP00000512825.1:n.*489-1G>A
ENST00000696709.1:n.1734G>A
ENST00000696710.1:c.1144-1G>A	ENSP00000512826.1:n.1144-1G>A
ENST00000696711.1:n.3202G>A
ENST00000696712.1:n.1260-26G>A
ENST00000696713.1:c.1144-1G>A	ENSP00000512827.1:n.1144-1G>A
ENST00000696714.1:n.1553-26G>A
ENST00000696715.1:c.1144-1G>A	ENSP00000512828.1:n.1144-1G>A