Canonical Allele Identifier: CA2133624555
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185323C= , CM000676.2:g.45185323C= GRCh38
NC_000014.8:g.45654526C= , CM000676.1:g.45654526C= GRCh37
NC_000014.7:g.44724276C= NCBI36
NG_007417.1:g.54391C= , LRG_502:g.54391C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2834C= ENSP00000450632.2:p.Ser945=
ENST00000555484.2:c.400C=
ENST00000556250.6:c.4415C= ENSP00000452033.2:p.Ser1472=
ENST00000557110.2:c.400C=
ENST00000696642.1:c.*3433C= ENSP00000512775.1:n.*3433C=
ENST00000696644.1:n.358C=
ENST00000696645.1:n.512C=
ENST00000696647.1:c.4622C= ENSP00000512778.1:p.Ser1541=
ENST00000696648.1:c.*2647C= ENSP00000512779.1:n.*2647C=
ENST00000696649.1:c.4466C= ENSP00000512780.1:p.Ser1489=
ENST00000696650.1:n.4570C=
ENST00000696659.1:c.2620C=
ENST00000696663.1:c.3553C=
ENST00000696664.1:c.3454C=
ENST00000696665.1:c.400C=
ENST00000696675.1:c.*378C= ENSP00000512799.1:n.*378C=
ENST00000696683.1:c.3439C=
ENST00000696684.1:c.3439C=
ENST00000696685.1:c.3439C=
ENST00000696686.1:n.1359C=
ENST00000267430.10:c.4622C= MANE Select ENSP00000267430.5:p.Ser1541=
ENST00000267430.9:c.4622C= ENSP00000267430.5:p.Ser1541=
ENST00000542564.6:c.4544C= ENSP00000442493.2:p.Ser1515=
ENST00000554809.5:c.1419C=
ENST00000555013.1:n.455C=
ENST00000556250.5:c.3170C= ENSP00000452033.1:p.Ser1057=
NM_001308133.1:c.4544C= NP_001295062.1:p.Ser1515=
NM_020937.2:c.4622C= , LRG_502t1:c.4622C= NP_065988.1:p.Ser1541=
NM_020937.3:c.4622C= NP_065988.1:p.Ser1541=
XM_011537034.1:c.4637C= XP_011535336.1:p.Ser1546=
XM_011537035.1:c.4559C= XP_011535337.1:p.Ser1520=
XM_011537036.1:c.4637C= XP_011535338.1:p.Ser1546=
XM_011537037.1:c.2651C= XP_011535339.1:p.Ser884=
XM_011537034.2:c.4637C= XP_011535336.1:p.Ser1546=
XM_011537035.3:c.4559C= XP_011535337.1:p.Ser1520=
XM_011537037.3:c.2651C= XP_011535339.1:p.Ser884=
XM_017021523.1:c.4637C= XP_016877012.1:p.Ser1546=
XM_017021524.2:c.3674C= XP_016877013.1:p.Ser1225=
XM_017021525.2:c.3452C= XP_016877014.1:p.Ser1151=
XM_017021526.2:c.3452C= XP_016877015.1:p.Ser1151=
XM_017021527.1:c.3437C= XP_016877016.1:p.Ser1146=
XR_001750470.1:n.4729C=
XR_001750471.2:n.4714C=
XR_001750472.1:n.4766C=
NM_020937.4:c.4622C= MANE Select NP_065988.1:p.Ser1541=
NM_001308133.2:c.4544C= NP_001295062.1:p.Ser1515=