Canonical Allele Identifier: CA373307143

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075519C>T , CM000671.2:g.35075519C>T	GRCh38
NC_000009.11:g.35075516C>T , CM000671.1:g.35075516C>T	GRCh37
NC_000009.10:g.35065516C>T	NCBI36
NG_007312.1:g.9498G>A , LRG_499:g.9498G>A
NG_007887.1:g.2224G>A , LRG_657:g.2224G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1379G>A MANE Select	NP_004620.1:p.Gly460Asp
ENST00000378643.8:c.1379G>A MANE Select	ENSP00000367910.4:p.Gly460Asp
NM_004629.1:c.1379G>A , LRG_499t1:c.1379G>A	NP_004620.1:p.Gly460Asp
ENST00000378643.7:c.1379G>A	ENSP00000367910.3:p.Gly460Asp
ENST00000425676.5:c.*855G>A	ENSP00000412793.1:n.*855G>A
ENST00000448890.2:c.1379G>A	ENSP00000409607.2:p.Gly460Asp
ENST00000461149.2:n.2571G>A
ENST00000476212.1:n.44+1003G>A
ENST00000696700.1:n.2606G>A
ENST00000696701.1:n.1483G>A
ENST00000696702.1:c.*830G>A	ENSP00000512821.1:n.*830G>A
ENST00000696703.1:c.*763G>A	ENSP00000512822.1:n.*763G>A
ENST00000696706.1:n.1442G>A
ENST00000696707.1:n.1596G>A
ENST00000696708.1:c.*724G>A	ENSP00000512825.1:n.*724G>A
ENST00000696709.1:n.1970G>A
ENST00000696710.1:c.1379G>A	ENSP00000512826.1:p.Gly460Asp
ENST00000696711.1:n.3438G>A
ENST00000696712.1:n.1470G>A
ENST00000696713.1:c.1379G>A	ENSP00000512827.1:p.Gly460Asp
ENST00000696714.1:n.1763G>A
ENST00000696715.1:c.1379G>A	ENSP00000512828.1:p.Gly460Asp