Canonical Allele Identifier: CA2133624574
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185338T= , CM000676.2:g.45185338T= GRCh38
NC_000014.8:g.45654541T= , CM000676.1:g.45654541T= GRCh37
NC_000014.7:g.44724291T= NCBI36
NG_007417.1:g.54406T= , LRG_502:g.54406T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2849T= ENSP00000450632.2:p.Leu950=
ENST00000555484.2:c.415T=
ENST00000556250.6:c.4430T= ENSP00000452033.2:p.Leu1477=
ENST00000557110.2:c.415T=
ENST00000696642.1:c.*3448T= ENSP00000512775.1:n.*3448T=
ENST00000696644.1:n.373T=
ENST00000696645.1:n.527T=
ENST00000696647.1:c.4637T= ENSP00000512778.1:p.Leu1546=
ENST00000696648.1:c.*2662T= ENSP00000512779.1:n.*2662T=
ENST00000696649.1:c.4481T= ENSP00000512780.1:p.Leu1494=
ENST00000696650.1:n.4585T=
ENST00000696659.1:c.2635T=
ENST00000696663.1:c.3568T=
ENST00000696664.1:c.3469T=
ENST00000696665.1:c.415T=
ENST00000696675.1:c.*393T= ENSP00000512799.1:n.*393T=
ENST00000696683.1:c.3454T=
ENST00000696684.1:c.3454T=
ENST00000696685.1:c.3454T=
ENST00000696686.1:n.1374T=
ENST00000267430.10:c.4637T= MANE Select ENSP00000267430.5:p.Leu1546=
ENST00000267430.9:c.4637T= ENSP00000267430.5:p.Leu1546=
ENST00000542564.6:c.4559T= ENSP00000442493.2:p.Leu1520=
ENST00000554809.5:c.1434T=
ENST00000555013.1:n.470T=
ENST00000556250.5:c.3185T= ENSP00000452033.1:p.Leu1062=
NM_001308133.1:c.4559T= NP_001295062.1:p.Leu1520=
NM_020937.2:c.4637T= , LRG_502t1:c.4637T= NP_065988.1:p.Leu1546=
NM_020937.3:c.4637T= NP_065988.1:p.Leu1546=
XM_011537034.1:c.4652T= XP_011535336.1:p.Leu1551=
XM_011537035.1:c.4574T= XP_011535337.1:p.Leu1525=
XM_011537036.1:c.4652T= XP_011535338.1:p.Leu1551=
XM_011537037.1:c.2666T= XP_011535339.1:p.Leu889=
XM_011537034.2:c.4652T= XP_011535336.1:p.Leu1551=
XM_011537035.3:c.4574T= XP_011535337.1:p.Leu1525=
XM_011537037.3:c.2666T= XP_011535339.1:p.Leu889=
XM_017021523.1:c.4652T= XP_016877012.1:p.Leu1551=
XM_017021524.2:c.3689T= XP_016877013.1:p.Leu1230=
XM_017021525.2:c.3467T= XP_016877014.1:p.Leu1156=
XM_017021526.2:c.3467T= XP_016877015.1:p.Leu1156=
XM_017021527.1:c.3452T= XP_016877016.1:p.Leu1151=
XR_001750470.1:n.4744T=
XR_001750471.2:n.4729T=
XR_001750472.1:n.4781T=
NM_020937.4:c.4637T= MANE Select NP_065988.1:p.Leu1546=
NM_001308133.2:c.4559T= NP_001295062.1:p.Leu1520=