Canonical Allele Identifier: CA159275

Gene: FANCA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89769915C>T , CM000678.2:g.89769915C>T	GRCh38
NC_000016.9:g.89836323C>T , CM000678.1:g.89836323C>T	GRCh37
NC_000016.8:g.88363824C>T	NCBI36
NG_011706.1:g.51743G>A , LRG_495:g.51743G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561667.2:c.*920G>A	ENSP00000512522.1:n.*920G>A
ENST00000564475.6:c.2426G>A	ENSP00000454977.2:p.Gly809Asp
ENST00000567205.2:c.2426G>A	ENSP00000457027.2:p.Gly809Asp
ENST00000567510.2:c.1125G>A	ENSP00000455969.1:n.1125G>A
ENST00000568369.6:c.2426G>A	ENSP00000456829.1:p.Gly809Asp
ENST00000696274.1:n.2387G>A
ENST00000696275.1:c.*1661G>A	ENSP00000512517.1:n.*1661G>A
ENST00000696276.1:n.2469G>A
ENST00000696286.1:c.2426G>A	ENSP00000512523.1:p.Gly809Asp
ENST00000696287.1:c.2426G>A	ENSP00000512524.1:p.Gly809Asp
ENST00000696291.1:c.*2146G>A	ENSP00000512530.1:n.*2146G>A
ENST00000389301.8:c.2426G>A MANE Select	ENSP00000373952.3:p.Gly809Asp
ENST00000389301.7:c.2426G>A	ENSP00000373952.3:p.Gly809Asp
ENST00000561667.1:n.528G>A
ENST00000567205.1:c.110G>A	ENSP00000457027.1:p.Gly37Asp
ENST00000568369.5:c.2426G>A	ENSP00000456829.1:p.Gly809Asp
NM_000135.2:c.2426G>A , LRG_495t1:c.2426G>A	NP_000126.2:p.Gly809Asp
NM_001286167.1:c.2426G>A	NP_001273096.1:p.Gly809Asp
XM_005256294.3:c.2426G>A	XP_005256351.1:p.Gly809Asp
XM_011522945.1:c.2426G>A	XP_011521247.1:p.Gly809Asp
XM_011522946.1:c.1403G>A	XP_011521248.1:p.Gly468Asp
XM_011522947.1:c.1403G>A	XP_011521249.1:p.Gly468Asp
XR_933244.1:n.2469G>A
XR_933245.1:n.2469G>A
XR_933246.1:n.2469G>A
XR_933247.1:n.2469G>A
NM_000135.3:c.2426G>A	NP_000126.2:p.Gly809Asp
NM_001286167.2:c.2426G>A	NP_001273096.1:p.Gly809Asp
XM_005256294.4:c.2426G>A	XP_005256351.1:p.Gly809Asp
XM_011522945.2:c.2426G>A	XP_011521247.1:p.Gly809Asp
XM_011522946.3:c.1403G>A	XP_011521248.1:p.Gly468Asp
XM_011522947.2:c.1403G>A	XP_011521249.1:p.Gly468Asp
XM_017023044.2:c.2426G>A	XP_016878533.1:p.Gly809Asp
XM_017023045.1:c.2426G>A	XP_016878534.1:p.Gly809Asp
XM_024450189.1:c.1403G>A	XP_024305957.1:p.Gly468Asp
XR_001751866.1:n.2469G>A
XR_933244.2:n.2469G>A
XR_933245.2:n.2469G>A
XR_933247.2:n.2469G>A
NM_000135.4:c.2426G>A MANE Select	NP_000126.2:p.Gly809Asp
NM_001286167.3:c.2426G>A	NP_001273096.1:p.Gly809Asp