Canonical Allele Identifier: CA2133607287
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45159233G= , CM000676.2:g.45159233G= GRCh38
NC_000014.8:g.45628436G= , CM000676.1:g.45628436G= GRCh37
NC_000014.7:g.44698186G= NCBI36
NG_007417.1:g.28301G= , LRG_502:g.28301G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000556036.6:c.1534G= ENSP00000450596.1:p.Ala512=
ENST00000556250.6:c.1534G= ENSP00000452033.2:p.Ala512=
ENST00000696641.1:c.1375G= ENSP00000512774.1:p.Ala459=
ENST00000696642.1:c.*345G= ENSP00000512775.1:n.*345G=
ENST00000696643.1:c.1534G= ENSP00000512776.1:p.Ala512=
ENST00000696646.1:c.*345G= ENSP00000512777.1:n.*345G=
ENST00000696647.1:c.1534G= ENSP00000512778.1:p.Ala512=
ENST00000696648.1:c.1534G= ENSP00000512779.1:p.Ala512=
ENST00000696649.1:c.1534G= ENSP00000512780.1:p.Ala512=
ENST00000696650.1:n.1482G=
ENST00000696658.1:n.2084G=
ENST00000696662.1:c.1456G= ENSP00000512788.1:p.Ala486=
ENST00000696663.1:c.351G=
ENST00000696664.1:c.351G=
ENST00000696675.1:c.1534G= ENSP00000512799.1:p.Ala512=
ENST00000696680.1:c.1402G= ENSP00000512803.1:p.Ala468=
ENST00000696681.1:c.*345G= ENSP00000512804.1:n.*345G=
ENST00000696682.1:c.1534G= ENSP00000512805.1:p.Ala512=
ENST00000696683.1:c.351G=
ENST00000696684.1:c.351G=
ENST00000696685.1:c.351G=
ENST00000267430.10:c.1534G= MANE Select ENSP00000267430.5:p.Ala512=
ENST00000267430.9:c.1534G= ENSP00000267430.5:p.Ala512=
ENST00000542564.6:c.1456G= ENSP00000442493.2:p.Ala486=
ENST00000556036.5:c.1534G= ENSP00000450596.1:p.Ala512=
ENST00000556250.5:c.289G= ENSP00000452033.1:p.Ala97=
NM_001308133.1:c.1456G= NP_001295062.1:p.Ala486=
NM_001308134.1:c.1534G= NP_001295063.1:p.Ala512=
NM_020937.2:c.1534G= , LRG_502t1:c.1534G= NP_065988.1:p.Ala512=
NM_020937.3:c.1534G= NP_065988.1:p.Ala512=
XM_011537034.1:c.1534G= XP_011535336.1:p.Ala512=
XM_011537035.1:c.1456G= XP_011535337.1:p.Ala486=
XM_011537036.1:c.1534G= XP_011535338.1:p.Ala512=
XM_011537034.2:c.1534G= XP_011535336.1:p.Ala512=
XM_011537035.3:c.1456G= XP_011535337.1:p.Ala486=
XM_017021523.1:c.1534G= XP_016877012.1:p.Ala512=
XM_017021524.2:c.571G= XP_016877013.1:p.Ala191=
XM_017021525.2:c.349G= XP_016877014.1:p.Ala117=
XM_017021526.2:c.349G= XP_016877015.1:p.Ala117=
XM_017021527.1:c.349G= XP_016877016.1:p.Ala117=
XR_001750470.1:n.1626G=
XR_001750471.2:n.1626G=
XR_001750472.1:n.1626G=
NM_020937.4:c.1534G= MANE Select NP_065988.1:p.Ala512=
NM_001308133.2:c.1456G= NP_001295062.1:p.Ala486=
NM_001308134.2:c.1534G= NP_001295063.1:p.Ala512=