Canonical Allele Identifier: CA5040140

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35079243T>A , CM000671.2:g.35079243T>A	GRCh38
NC_000009.11:g.35079240T>A , CM000671.1:g.35079240T>A	GRCh37
NC_000009.10:g.35069240T>A	NCBI36
NG_007312.1:g.5774A>T , LRG_499:g.5774A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.85-2A>T MANE Select	NP_004620.1:n.85-2A>T
ENST00000378643.8:c.85-2A>T MANE Select	ENSP00000367910.4:n.85-2A>T
NM_004629.1:c.85-2A>T , LRG_499t1:c.85-2A>T	NP_004620.1:n.85-2A>T
ENST00000378643.7:c.85-2A>T	ENSP00000367910.3:n.85-2A>T
ENST00000425676.5:c.85-2A>T	ENSP00000412793.1:n.85-2A>T
ENST00000448890.1:c.85-2A>T	ENSP00000409607.1:n.85-2A>T
ENST00000448890.2:c.85-2A>T	ENSP00000409607.2:n.85-2A>T
ENST00000461149.2:n.561-2A>T
ENST00000462124.1:n.427A>T
ENST00000696700.1:n.335-2A>T
ENST00000696701.1:n.300-2A>T
ENST00000696702.1:c.85-2A>T	ENSP00000512821.1:n.85-2A>T
ENST00000696703.1:c.85-2A>T	ENSP00000512822.1:n.85-2A>T
ENST00000696707.1:n.41-2A>T
ENST00000696708.1:c.85-2A>T	ENSP00000512825.1:n.85-2A>T
ENST00000696709.1:n.487-2A>T
ENST00000696710.1:c.85-2A>T	ENSP00000512826.1:n.85-2A>T
ENST00000696711.1:n.432-2A>T
ENST00000696713.1:c.85-2A>T	ENSP00000512827.1:n.85-2A>T
ENST00000696714.1:n.762A>T
ENST00000696715.1:c.85-2A>T	ENSP00000512828.1:n.85-2A>T