Canonical Allele Identifier: CA373304200

Gene: FANCG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35075002C>A , CM000671.2:g.35075002C>A	GRCh38
NC_000009.11:g.35074999C>A , CM000671.1:g.35074999C>A	GRCh37
NC_000009.10:g.35064999C>A	NCBI36
NG_007312.1:g.10015G>T , LRG_499:g.10015G>T
NG_007887.1:g.2741G>T , LRG_657:g.2741G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004629.2:c.1561G>T MANE Select	NP_004620.1:p.Gly521Ter
ENST00000378643.8:c.1561G>T MANE Select	ENSP00000367910.4:p.Gly521Ter
NM_004629.1:c.1561G>T , LRG_499t1:c.1561G>T	NP_004620.1:p.Gly521Ter
ENST00000378643.7:c.1561G>T	ENSP00000367910.3:p.Gly521Ter
ENST00000425676.5:c.*1037G>T	ENSP00000412793.1:n.*1037G>T
ENST00000448890.2:c.1561G>T	ENSP00000409607.2:p.Gly521Ter
ENST00000461149.2:n.2949G>T
ENST00000476212.1:n.45-570G>T
ENST00000481254.1:n.369G>T
ENST00000696700.1:n.2984G>T
ENST00000696701.1:n.1861G>T
ENST00000696702.1:c.*1012G>T	ENSP00000512821.1:n.*1012G>T
ENST00000696703.1:c.*945G>T	ENSP00000512822.1:n.*945G>T
ENST00000696706.1:n.1624G>T
ENST00000696707.1:n.1778G>T
ENST00000696708.1:c.*906G>T	ENSP00000512825.1:n.*906G>T
ENST00000696709.1:n.2348G>T
ENST00000696710.1:c.1555G>T	ENSP00000512826.1:p.Gly519Ter
ENST00000696711.1:n.3816G>T
ENST00000696712.1:n.1848G>T
ENST00000696713.1:c.1561G>T	ENSP00000512827.1:p.Gly521Ter
ENST00000696714.1:n.2141G>T
ENST00000696715.1:c.1561G>T	ENSP00000512828.1:p.Gly521Ter