Canonical Allele Identifier: CA373307424

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075546C>T , CM000671.2:g.35075546C>T	GRCh38
NC_000009.11:g.35075543C>T , CM000671.1:g.35075543C>T	GRCh37
NC_000009.10:g.35065543C>T	NCBI36
NG_007312.1:g.9471G>A , LRG_499:g.9471G>A
NG_007887.1:g.2197G>A , LRG_657:g.2197G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1352G>A MANE Select	NP_004620.1:p.Trp451Ter
ENST00000378643.8:c.1352G>A MANE Select	ENSP00000367910.4:p.Trp451Ter
NM_004629.1:c.1352G>A , LRG_499t1:c.1352G>A	NP_004620.1:p.Trp451Ter
ENST00000378643.7:c.1352G>A	ENSP00000367910.3:p.Trp451Ter
ENST00000425676.5:c.*828G>A	ENSP00000412793.1:n.*828G>A
ENST00000448890.2:c.1352G>A	ENSP00000409607.2:p.Trp451Ter
ENST00000461149.2:n.2544G>A
ENST00000476212.1:n.44+976G>A
ENST00000696700.1:n.2579G>A
ENST00000696701.1:n.1456G>A
ENST00000696702.1:c.*803G>A	ENSP00000512821.1:n.*803G>A
ENST00000696703.1:c.*736G>A	ENSP00000512822.1:n.*736G>A
ENST00000696706.1:n.1415G>A
ENST00000696707.1:n.1569G>A
ENST00000696708.1:c.*697G>A	ENSP00000512825.1:n.*697G>A
ENST00000696709.1:n.1943G>A
ENST00000696710.1:c.1352G>A	ENSP00000512826.1:p.Trp451Ter
ENST00000696711.1:n.3411G>A
ENST00000696712.1:n.1443G>A
ENST00000696713.1:c.1352G>A	ENSP00000512827.1:p.Trp451Ter
ENST00000696714.1:n.1736G>A
ENST00000696715.1:c.1352G>A	ENSP00000512828.1:p.Trp451Ter