Canonical Allele Identifier: CA2133624474
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185250G= , CM000676.2:g.45185250G= GRCh38
NC_000014.8:g.45654453G= , CM000676.1:g.45654453G= GRCh37
NC_000014.7:g.44724203G= NCBI36
NG_007417.1:g.54318G= , LRG_502:g.54318G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2761G= ENSP00000450632.2:p.Glu921=
ENST00000555484.2:c.327G=
ENST00000556250.6:c.4342G= ENSP00000452033.2:p.Glu1448=
ENST00000557110.2:c.327G=
ENST00000696642.1:c.*3360G= ENSP00000512775.1:n.*3360G=
ENST00000696644.1:n.285G=
ENST00000696645.1:n.439G=
ENST00000696647.1:c.4549G= ENSP00000512778.1:p.Glu1517=
ENST00000696648.1:c.*2574G= ENSP00000512779.1:n.*2574G=
ENST00000696649.1:c.4393G= ENSP00000512780.1:p.Glu1465=
ENST00000696650.1:n.4497G=
ENST00000696659.1:c.2547G=
ENST00000696663.1:c.3480G=
ENST00000696664.1:c.3381G=
ENST00000696665.1:c.327G=
ENST00000696675.1:c.*305G= ENSP00000512799.1:n.*305G=
ENST00000696683.1:c.3366G=
ENST00000696684.1:c.3366G=
ENST00000696685.1:c.3366G=
ENST00000696686.1:n.1286G=
ENST00000267430.10:c.4549G= MANE Select ENSP00000267430.5:p.Glu1517=
ENST00000267430.9:c.4549G= ENSP00000267430.5:p.Glu1517=
ENST00000542564.6:c.4471G= ENSP00000442493.2:p.Glu1491=
ENST00000554809.5:c.1346G=
ENST00000555013.1:n.382G=
ENST00000556250.5:c.3097G= ENSP00000452033.1:p.Glu1033=
NM_001308133.1:c.4471G= NP_001295062.1:p.Glu1491=
NM_020937.2:c.4549G= , LRG_502t1:c.4549G= NP_065988.1:p.Glu1517=
NM_020937.3:c.4549G= NP_065988.1:p.Glu1517=
XM_011537034.1:c.4564G= XP_011535336.1:p.Glu1522=
XM_011537035.1:c.4486G= XP_011535337.1:p.Glu1496=
XM_011537036.1:c.4564G= XP_011535338.1:p.Glu1522=
XM_011537037.1:c.2578G= XP_011535339.1:p.Glu860=
XM_011537034.2:c.4564G= XP_011535336.1:p.Glu1522=
XM_011537035.3:c.4486G= XP_011535337.1:p.Glu1496=
XM_011537037.3:c.2578G= XP_011535339.1:p.Glu860=
XM_017021523.1:c.4564G= XP_016877012.1:p.Glu1522=
XM_017021524.2:c.3601G= XP_016877013.1:p.Glu1201=
XM_017021525.2:c.3379G= XP_016877014.1:p.Glu1127=
XM_017021526.2:c.3379G= XP_016877015.1:p.Glu1127=
XM_017021527.1:c.3364G= XP_016877016.1:p.Glu1122=
XR_001750470.1:n.4656G=
XR_001750471.2:n.4641G=
XR_001750472.1:n.4693G=
NM_020937.4:c.4549G= MANE Select NP_065988.1:p.Glu1517=
NM_001308133.2:c.4471G= NP_001295062.1:p.Glu1491=