Canonical Allele Identifier: CA2133624572
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185336T= , CM000676.2:g.45185336T= GRCh38
NC_000014.8:g.45654539T= , CM000676.1:g.45654539T= GRCh37
NC_000014.7:g.44724289T= NCBI36
NG_007417.1:g.54404T= , LRG_502:g.54404T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2847T= ENSP00000450632.2:p.Phe949=
ENST00000555484.2:c.413T=
ENST00000556250.6:c.4428T= ENSP00000452033.2:p.Phe1476=
ENST00000557110.2:c.413T=
ENST00000696642.1:c.*3446T= ENSP00000512775.1:n.*3446T=
ENST00000696644.1:n.371T=
ENST00000696645.1:n.525T=
ENST00000696647.1:c.4635T= ENSP00000512778.1:p.Phe1545=
ENST00000696648.1:c.*2660T= ENSP00000512779.1:n.*2660T=
ENST00000696649.1:c.4479T= ENSP00000512780.1:p.Phe1493=
ENST00000696650.1:n.4583T=
ENST00000696659.1:c.2633T=
ENST00000696663.1:c.3566T=
ENST00000696664.1:c.3467T=
ENST00000696665.1:c.413T=
ENST00000696675.1:c.*391T= ENSP00000512799.1:n.*391T=
ENST00000696683.1:c.3452T=
ENST00000696684.1:c.3452T=
ENST00000696685.1:c.3452T=
ENST00000696686.1:n.1372T=
ENST00000267430.10:c.4635T= MANE Select ENSP00000267430.5:p.Phe1545=
ENST00000267430.9:c.4635T= ENSP00000267430.5:p.Phe1545=
ENST00000542564.6:c.4557T= ENSP00000442493.2:p.Phe1519=
ENST00000554809.5:c.1432T=
ENST00000555013.1:n.468T=
ENST00000556250.5:c.3183T= ENSP00000452033.1:p.Phe1061=
NM_001308133.1:c.4557T= NP_001295062.1:p.Phe1519=
NM_020937.2:c.4635T= , LRG_502t1:c.4635T= NP_065988.1:p.Phe1545=
NM_020937.3:c.4635T= NP_065988.1:p.Phe1545=
XM_011537034.1:c.4650T= XP_011535336.1:p.Phe1550=
XM_011537035.1:c.4572T= XP_011535337.1:p.Phe1524=
XM_011537036.1:c.4650T= XP_011535338.1:p.Phe1550=
XM_011537037.1:c.2664T= XP_011535339.1:p.Phe888=
XM_011537034.2:c.4650T= XP_011535336.1:p.Phe1550=
XM_011537035.3:c.4572T= XP_011535337.1:p.Phe1524=
XM_011537037.3:c.2664T= XP_011535339.1:p.Phe888=
XM_017021523.1:c.4650T= XP_016877012.1:p.Phe1550=
XM_017021524.2:c.3687T= XP_016877013.1:p.Phe1229=
XM_017021525.2:c.3465T= XP_016877014.1:p.Phe1155=
XM_017021526.2:c.3465T= XP_016877015.1:p.Phe1155=
XM_017021527.1:c.3450T= XP_016877016.1:p.Phe1150=
XR_001750470.1:n.4742T=
XR_001750471.2:n.4727T=
XR_001750472.1:n.4779T=
NM_020937.4:c.4635T= MANE Select NP_065988.1:p.Phe1545=
NM_001308133.2:c.4557T= NP_001295062.1:p.Phe1519=