Canonical Allele Identifier: CA464415689

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35077361A>G , CM000671.2:g.35077361A>G	GRCh38
NC_000009.11:g.35077358A>G , CM000671.1:g.35077358A>G	GRCh37
NC_000009.10:g.35067358A>G	NCBI36
NG_007312.1:g.7656T>C , LRG_499:g.7656T>C
NG_007887.1:g.382T>C , LRG_657:g.382T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.549T>C	ENSP00000409607.2:p.Thr183=
ENST00000461149.2:n.1766T>C
ENST00000696700.1:n.1801T>C
ENST00000696701.1:n.653T>C
ENST00000696702.1:c.*25T>C	ENSP00000512821.1:n.*25T>C
ENST00000696703.1:c.*25T>C	ENSP00000512822.1:n.*25T>C
ENST00000696706.1:n.612T>C
ENST00000696707.1:n.766T>C
ENST00000696708.1:c.*25T>C	ENSP00000512825.1:n.*25T>C
ENST00000696709.1:n.951T>C
ENST00000696710.1:c.549T>C	ENSP00000512826.1:p.Thr183=
ENST00000696711.1:n.1898T>C
ENST00000696712.1:n.636T>C
ENST00000696713.1:c.549T>C	ENSP00000512827.1:p.Thr183=
ENST00000696714.1:n.1025T>C
ENST00000696715.1:c.549T>C	ENSP00000512828.1:p.Thr183=
ENST00000378643.8:c.549T>C MANE Select	ENSP00000367910.4:p.Thr183=
ENST00000378643.7:c.549T>C	ENSP00000367910.3:p.Thr183=
ENST00000425676.5:c.*25T>C	ENSP00000412793.1:n.*25T>C
ENST00000448890.1:c.549T>C	ENSP00000409607.1:p.Thr183=
NM_004629.1:c.549T>C , LRG_499t1:c.549T>C	NP_004620.1:p.Thr183=
NM_004629.2:c.549T>C MANE Select	NP_004620.1:p.Thr183=