Canonical Allele Identifier: CA373301212

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35074474G>A , CM000671.2:g.35074474G>A	GRCh38
NC_000009.11:g.35074471G>A , CM000671.1:g.35074471G>A	GRCh37
NC_000009.10:g.35064471G>A	NCBI36
NG_007312.1:g.10543C>T , LRG_499:g.10543C>T
NG_007887.1:g.3269C>T , LRG_657:g.3269C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448890.2:c.1657C>T	ENSP00000409607.2:p.His553Tyr
ENST00000461149.2:n.3477C>T
ENST00000696700.1:n.3512C>T
ENST00000696701.1:n.1957C>T
ENST00000696702.1:c.*1108C>T	ENSP00000512821.1:n.*1108C>T
ENST00000696703.1:c.*1041C>T	ENSP00000512822.1:n.*1041C>T
ENST00000696706.1:n.1720C>T
ENST00000696707.1:n.1874C>T
ENST00000696708.1:c.*1002C>T	ENSP00000512825.1:n.*1002C>T
ENST00000696709.1:n.2876C>T
ENST00000696710.1:c.1651C>T	ENSP00000512826.1:p.His551Tyr
ENST00000696711.1:n.4344C>T
ENST00000696712.1:n.2376C>T
ENST00000696713.1:c.1637-12C>T	ENSP00000512827.1:n.1637-12C>T
ENST00000696714.1:n.2669C>T
ENST00000696715.1:c.1657C>T	ENSP00000512828.1:p.His553Tyr
ENST00000378643.8:c.1657C>T MANE Select	ENSP00000367910.4:p.His553Tyr
ENST00000378643.7:c.1657C>T	ENSP00000367910.3:p.His553Tyr
ENST00000425676.5:c.*1133C>T	ENSP00000412793.1:n.*1133C>T
ENST00000476212.1:n.45-42C>T
NM_004629.1:c.1657C>T , LRG_499t1:c.1657C>T	NP_004620.1:p.His553Tyr
NM_004629.2:c.1657C>T MANE Select	NP_004620.1:p.His553Tyr