Canonical Allele Identifier: CA2133624483
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185261A= , CM000676.2:g.45185261A= GRCh38
NC_000014.8:g.45654464A= , CM000676.1:g.45654464A= GRCh37
NC_000014.7:g.44724214A= NCBI36
NG_007417.1:g.54329A= , LRG_502:g.54329A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2772A= ENSP00000450632.2:p.Glu924=
ENST00000555484.2:c.338A=
ENST00000556250.6:c.4353A= ENSP00000452033.2:p.Glu1451=
ENST00000557110.2:c.338A=
ENST00000696642.1:c.*3371A= ENSP00000512775.1:n.*3371A=
ENST00000696644.1:n.296A=
ENST00000696645.1:n.450A=
ENST00000696647.1:c.4560A= ENSP00000512778.1:p.Glu1520=
ENST00000696648.1:c.*2585A= ENSP00000512779.1:n.*2585A=
ENST00000696649.1:c.4404A= ENSP00000512780.1:p.Glu1468=
ENST00000696650.1:n.4508A=
ENST00000696659.1:c.2558A=
ENST00000696663.1:c.3491A=
ENST00000696664.1:c.3392A=
ENST00000696665.1:c.338A=
ENST00000696675.1:c.*316A= ENSP00000512799.1:n.*316A=
ENST00000696683.1:c.3377A=
ENST00000696684.1:c.3377A=
ENST00000696685.1:c.3377A=
ENST00000696686.1:n.1297A=
ENST00000267430.10:c.4560A= MANE Select ENSP00000267430.5:p.Glu1520=
ENST00000267430.9:c.4560A= ENSP00000267430.5:p.Glu1520=
ENST00000542564.6:c.4482A= ENSP00000442493.2:p.Glu1494=
ENST00000554809.5:c.1357A=
ENST00000555013.1:n.393A=
ENST00000556250.5:c.3108A= ENSP00000452033.1:p.Glu1036=
NM_001308133.1:c.4482A= NP_001295062.1:p.Glu1494=
NM_020937.2:c.4560A= , LRG_502t1:c.4560A= NP_065988.1:p.Glu1520=
NM_020937.3:c.4560A= NP_065988.1:p.Glu1520=
XM_011537034.1:c.4575A= XP_011535336.1:p.Glu1525=
XM_011537035.1:c.4497A= XP_011535337.1:p.Glu1499=
XM_011537036.1:c.4575A= XP_011535338.1:p.Glu1525=
XM_011537037.1:c.2589A= XP_011535339.1:p.Glu863=
XM_011537034.2:c.4575A= XP_011535336.1:p.Glu1525=
XM_011537035.3:c.4497A= XP_011535337.1:p.Glu1499=
XM_011537037.3:c.2589A= XP_011535339.1:p.Glu863=
XM_017021523.1:c.4575A= XP_016877012.1:p.Glu1525=
XM_017021524.2:c.3612A= XP_016877013.1:p.Glu1204=
XM_017021525.2:c.3390A= XP_016877014.1:p.Glu1130=
XM_017021526.2:c.3390A= XP_016877015.1:p.Glu1130=
XM_017021527.1:c.3375A= XP_016877016.1:p.Glu1125=
XR_001750470.1:n.4667A=
XR_001750471.2:n.4652A=
XR_001750472.1:n.4704A=
NM_020937.4:c.4560A= MANE Select NP_065988.1:p.Glu1520=
NM_001308133.2:c.4482A= NP_001295062.1:p.Glu1494=