Canonical Allele Identifier: CA2133624546
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185318T= , CM000676.2:g.45185318T= GRCh38
NC_000014.8:g.45654521T= , CM000676.1:g.45654521T= GRCh37
NC_000014.7:g.44724271T= NCBI36
NG_007417.1:g.54386T= , LRG_502:g.54386T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2829T= ENSP00000450632.2:p.Asp943=
ENST00000555484.2:c.395T=
ENST00000556250.6:c.4410T= ENSP00000452033.2:p.Asp1470=
ENST00000557110.2:c.395T=
ENST00000696642.1:c.*3428T= ENSP00000512775.1:n.*3428T=
ENST00000696644.1:n.353T=
ENST00000696645.1:n.507T=
ENST00000696647.1:c.4617T= ENSP00000512778.1:p.Asp1539=
ENST00000696648.1:c.*2642T= ENSP00000512779.1:n.*2642T=
ENST00000696649.1:c.4461T= ENSP00000512780.1:p.Asp1487=
ENST00000696650.1:n.4565T=
ENST00000696659.1:c.2615T=
ENST00000696663.1:c.3548T=
ENST00000696664.1:c.3449T=
ENST00000696665.1:c.395T=
ENST00000696675.1:c.*373T= ENSP00000512799.1:n.*373T=
ENST00000696683.1:c.3434T=
ENST00000696684.1:c.3434T=
ENST00000696685.1:c.3434T=
ENST00000696686.1:n.1354T=
ENST00000267430.10:c.4617T= MANE Select ENSP00000267430.5:p.Asp1539=
ENST00000267430.9:c.4617T= ENSP00000267430.5:p.Asp1539=
ENST00000542564.6:c.4539T= ENSP00000442493.2:p.Asp1513=
ENST00000554809.5:c.1414T=
ENST00000555013.1:n.450T=
ENST00000556250.5:c.3165T= ENSP00000452033.1:p.Asp1055=
NM_001308133.1:c.4539T= NP_001295062.1:p.Asp1513=
NM_020937.2:c.4617T= , LRG_502t1:c.4617T= NP_065988.1:p.Asp1539=
NM_020937.3:c.4617T= NP_065988.1:p.Asp1539=
XM_011537034.1:c.4632T= XP_011535336.1:p.Asp1544=
XM_011537035.1:c.4554T= XP_011535337.1:p.Asp1518=
XM_011537036.1:c.4632T= XP_011535338.1:p.Asp1544=
XM_011537037.1:c.2646T= XP_011535339.1:p.Asp882=
XM_011537034.2:c.4632T= XP_011535336.1:p.Asp1544=
XM_011537035.3:c.4554T= XP_011535337.1:p.Asp1518=
XM_011537037.3:c.2646T= XP_011535339.1:p.Asp882=
XM_017021523.1:c.4632T= XP_016877012.1:p.Asp1544=
XM_017021524.2:c.3669T= XP_016877013.1:p.Asp1223=
XM_017021525.2:c.3447T= XP_016877014.1:p.Asp1149=
XM_017021526.2:c.3447T= XP_016877015.1:p.Asp1149=
XM_017021527.1:c.3432T= XP_016877016.1:p.Asp1144=
XR_001750470.1:n.4724T=
XR_001750471.2:n.4709T=
XR_001750472.1:n.4761T=
NM_020937.4:c.4617T= MANE Select NP_065988.1:p.Asp1539=
NM_001308133.2:c.4539T= NP_001295062.1:p.Asp1513=