Canonical Allele Identifier: CA5040177

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35079543C>T , CM000671.2:g.35079543C>T	GRCh38
NC_000009.11:g.35079540C>T , CM000671.1:g.35079540C>T	GRCh37
NC_000009.10:g.35069540C>T	NCBI36
NG_007312.1:g.5474G>A , LRG_499:g.5474G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.-11-8G>A	ENSP00000409607.2:n.-11-8G>A
ENST00000461149.2:n.458G>A
ENST00000696700.1:n.240-8G>A
ENST00000696701.1:n.197G>A
ENST00000696702.1:c.-19G>A	ENSP00000512821.1:n.-19G>A
ENST00000696703.1:c.-19G>A	ENSP00000512822.1:n.-19G>A
ENST00000696708.1:c.-19G>A	ENSP00000512825.1:n.-19G>A
ENST00000696709.1:n.384G>A
ENST00000696710.1:c.-19G>A	ENSP00000512826.1:n.-19G>A
ENST00000696711.1:n.329G>A
ENST00000696713.1:c.-19G>A	ENSP00000512827.1:n.-19G>A
ENST00000696714.1:n.462G>A
ENST00000696715.1:c.-19G>A	ENSP00000512828.1:n.-19G>A
ENST00000378643.8:c.-19G>A MANE Select	ENSP00000367910.4:n.-19G>A
ENST00000378643.7:c.-19G>A	ENSP00000367910.3:n.-19G>A
ENST00000425676.5:c.-19G>A	ENSP00000412793.1:n.-19G>A
ENST00000448890.1:c.-11-8G>A	ENSP00000409607.1:n.-11-8G>A
ENST00000462124.1:n.127G>A
NM_004629.1:c.-19G>A , LRG_499t1:c.-19G>A	NP_004620.1:n.-19G>A
NM_004629.2:c.-19G>A MANE Select	NP_004620.1:n.-19G>A