Canonical Allele Identifier: CA373314545

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35078286C>T , CM000671.2:g.35078286C>T	GRCh38
NC_000009.11:g.35078283C>T , CM000671.1:g.35078283C>T	GRCh37
NC_000009.10:g.35068283C>T	NCBI36
NG_007312.1:g.6731G>A , LRG_499:g.6731G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.365G>A MANE Select	NP_004620.1:p.Trp122Ter
ENST00000378643.8:c.365G>A MANE Select	ENSP00000367910.4:p.Trp122Ter
NM_004629.1:c.365G>A , LRG_499t1:c.365G>A	NP_004620.1:p.Trp122Ter
ENST00000378643.7:c.365G>A	ENSP00000367910.3:p.Trp122Ter
ENST00000425676.5:c.307+319G>A	ENSP00000412793.1:n.307+319G>A
ENST00000448890.1:c.365G>A	ENSP00000409607.1:p.Trp122Ter
ENST00000448890.2:c.365G>A	ENSP00000409607.2:p.Trp122Ter
ENST00000461149.1:n.100G>A
ENST00000461149.2:n.841G>A
ENST00000696700.1:n.876G>A
ENST00000696701.1:n.523-209G>A
ENST00000696702.1:c.307+319G>A	ENSP00000512821.1:n.307+319G>A
ENST00000696703.1:c.307+319G>A	ENSP00000512822.1:n.307+319G>A
ENST00000696706.1:n.428G>A
ENST00000696707.1:n.582G>A
ENST00000696708.1:c.307+319G>A	ENSP00000512825.1:n.307+319G>A
ENST00000696709.1:n.767G>A
ENST00000696710.1:c.365G>A	ENSP00000512826.1:p.Trp122Ter
ENST00000696711.1:n.973G>A
ENST00000696713.1:c.365G>A	ENSP00000512827.1:p.Trp122Ter
ENST00000696714.1:n.986+319G>A
ENST00000696715.1:c.365G>A	ENSP00000512828.1:p.Trp122Ter