Canonical Allele Identifier: CA373305269

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075083C>G , CM000671.2:g.35075083C>G	GRCh38
NC_000009.11:g.35075080C>G , CM000671.1:g.35075080C>G	GRCh37
NC_000009.10:g.35065080C>G	NCBI36
NG_007312.1:g.9934G>C , LRG_499:g.9934G>C
NG_007887.1:g.2660G>C , LRG_657:g.2660G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1481-1G>C MANE Select	NP_004620.1:n.1481-1G>C
ENST00000378643.8:c.1481-1G>C MANE Select	ENSP00000367910.4:n.1481-1G>C
NM_004629.1:c.1481-1G>C , LRG_499t1:c.1481-1G>C	NP_004620.1:n.1481-1G>C
ENST00000378643.7:c.1481-1G>C	ENSP00000367910.3:n.1481-1G>C
ENST00000425676.5:c.*957-1G>C	ENSP00000412793.1:n.*957-1G>C
ENST00000448890.2:c.1481-1G>C	ENSP00000409607.2:n.1481-1G>C
ENST00000461149.2:n.2868G>C
ENST00000476212.1:n.45-651G>C
ENST00000481254.1:n.288G>C
ENST00000696700.1:n.2903G>C
ENST00000696701.1:n.1780G>C
ENST00000696702.1:c.*932-1G>C	ENSP00000512821.1:n.*932-1G>C
ENST00000696703.1:c.*865-1G>C	ENSP00000512822.1:n.*865-1G>C
ENST00000696706.1:n.1544-1G>C
ENST00000696707.1:n.1698-1G>C
ENST00000696708.1:c.*826-1G>C	ENSP00000512825.1:n.*826-1G>C
ENST00000696709.1:n.2267G>C
ENST00000696710.1:c.1481-7G>C	ENSP00000512826.1:n.1481-7G>C
ENST00000696711.1:n.3735G>C
ENST00000696712.1:n.1767G>C
ENST00000696713.1:c.1481-1G>C	ENSP00000512827.1:n.1481-1G>C
ENST00000696714.1:n.2060G>C
ENST00000696715.1:c.1481-1G>C	ENSP00000512828.1:n.1481-1G>C