Canonical Allele Identifier: CA2133624471
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185248C= , CM000676.2:g.45185248C= GRCh38
NC_000014.8:g.45654451C= , CM000676.1:g.45654451C= GRCh37
NC_000014.7:g.44724201C= NCBI36
NG_007417.1:g.54316C= , LRG_502:g.54316C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2759C= ENSP00000450632.2:p.Ala920=
ENST00000555484.2:c.325C=
ENST00000556250.6:c.4340C= ENSP00000452033.2:p.Ala1447=
ENST00000557110.2:c.325C=
ENST00000696642.1:c.*3358C= ENSP00000512775.1:n.*3358C=
ENST00000696644.1:n.283C=
ENST00000696645.1:n.437C=
ENST00000696647.1:c.4547C= ENSP00000512778.1:p.Ala1516=
ENST00000696648.1:c.*2572C= ENSP00000512779.1:n.*2572C=
ENST00000696649.1:c.4391C= ENSP00000512780.1:p.Ala1464=
ENST00000696650.1:n.4495C=
ENST00000696659.1:c.2545C=
ENST00000696663.1:c.3478C=
ENST00000696664.1:c.3379C=
ENST00000696665.1:c.325C=
ENST00000696675.1:c.*303C= ENSP00000512799.1:n.*303C=
ENST00000696683.1:c.3364C=
ENST00000696684.1:c.3364C=
ENST00000696685.1:c.3364C=
ENST00000696686.1:n.1284C=
ENST00000267430.10:c.4547C= MANE Select ENSP00000267430.5:p.Ala1516=
ENST00000267430.9:c.4547C= ENSP00000267430.5:p.Ala1516=
ENST00000542564.6:c.4469C= ENSP00000442493.2:p.Ala1490=
ENST00000554809.5:c.1344C=
ENST00000555013.1:n.380C=
ENST00000556250.5:c.3095C= ENSP00000452033.1:p.Ala1032=
NM_001308133.1:c.4469C= NP_001295062.1:p.Ala1490=
NM_020937.2:c.4547C= , LRG_502t1:c.4547C= NP_065988.1:p.Ala1516=
NM_020937.3:c.4547C= NP_065988.1:p.Ala1516=
XM_011537034.1:c.4562C= XP_011535336.1:p.Ala1521=
XM_011537035.1:c.4484C= XP_011535337.1:p.Ala1495=
XM_011537036.1:c.4562C= XP_011535338.1:p.Ala1521=
XM_011537037.1:c.2576C= XP_011535339.1:p.Ala859=
XM_011537034.2:c.4562C= XP_011535336.1:p.Ala1521=
XM_011537035.3:c.4484C= XP_011535337.1:p.Ala1495=
XM_011537037.3:c.2576C= XP_011535339.1:p.Ala859=
XM_017021523.1:c.4562C= XP_016877012.1:p.Ala1521=
XM_017021524.2:c.3599C= XP_016877013.1:p.Ala1200=
XM_017021525.2:c.3377C= XP_016877014.1:p.Ala1126=
XM_017021526.2:c.3377C= XP_016877015.1:p.Ala1126=
XM_017021527.1:c.3362C= XP_016877016.1:p.Ala1121=
XR_001750470.1:n.4654C=
XR_001750471.2:n.4639C=
XR_001750472.1:n.4691C=
NM_020937.4:c.4547C= MANE Select NP_065988.1:p.Ala1516=
NM_001308133.2:c.4469C= NP_001295062.1:p.Ala1490=