Canonical Allele Identifier: CA2133624457
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185237A= , CM000676.2:g.45185237A= GRCh38
NC_000014.8:g.45654440A= , CM000676.1:g.45654440A= GRCh37
NC_000014.7:g.44724190A= NCBI36
NG_007417.1:g.54305A= , LRG_502:g.54305A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2748A= ENSP00000450632.2:p.Leu916=
ENST00000555484.2:c.314A=
ENST00000556250.6:c.4329A= ENSP00000452033.2:p.Leu1443=
ENST00000557110.2:c.314A=
ENST00000696642.1:c.*3347A= ENSP00000512775.1:n.*3347A=
ENST00000696644.1:n.272A=
ENST00000696645.1:n.426A=
ENST00000696647.1:c.4536A= ENSP00000512778.1:p.Leu1512=
ENST00000696648.1:c.*2561A= ENSP00000512779.1:n.*2561A=
ENST00000696649.1:c.4380A= ENSP00000512780.1:p.Leu1460=
ENST00000696650.1:n.4484A=
ENST00000696659.1:c.2534A=
ENST00000696663.1:c.3467A=
ENST00000696664.1:c.3368A=
ENST00000696665.1:c.314A=
ENST00000696675.1:c.*292A= ENSP00000512799.1:n.*292A=
ENST00000696683.1:c.3353A=
ENST00000696684.1:c.3353A=
ENST00000696685.1:c.3353A=
ENST00000696686.1:n.1273A=
ENST00000267430.10:c.4536A= MANE Select ENSP00000267430.5:p.Leu1512=
ENST00000267430.9:c.4536A= ENSP00000267430.5:p.Leu1512=
ENST00000542564.6:c.4458A= ENSP00000442493.2:p.Leu1486=
ENST00000554809.5:c.1333A=
ENST00000555013.1:n.369A=
ENST00000556250.5:c.3084A= ENSP00000452033.1:p.Leu1028=
NM_001308133.1:c.4458A= NP_001295062.1:p.Leu1486=
NM_020937.2:c.4536A= , LRG_502t1:c.4536A= NP_065988.1:p.Leu1512=
NM_020937.3:c.4536A= NP_065988.1:p.Leu1512=
XM_011537034.1:c.4551A= XP_011535336.1:p.Leu1517=
XM_011537035.1:c.4473A= XP_011535337.1:p.Leu1491=
XM_011537036.1:c.4551A= XP_011535338.1:p.Leu1517=
XM_011537037.1:c.2565A= XP_011535339.1:p.Leu855=
XM_011537034.2:c.4551A= XP_011535336.1:p.Leu1517=
XM_011537035.3:c.4473A= XP_011535337.1:p.Leu1491=
XM_011537037.3:c.2565A= XP_011535339.1:p.Leu855=
XM_017021523.1:c.4551A= XP_016877012.1:p.Leu1517=
XM_017021524.2:c.3588A= XP_016877013.1:p.Leu1196=
XM_017021525.2:c.3366A= XP_016877014.1:p.Leu1122=
XM_017021526.2:c.3366A= XP_016877015.1:p.Leu1122=
XM_017021527.1:c.3351A= XP_016877016.1:p.Leu1117=
XR_001750470.1:n.4643A=
XR_001750471.2:n.4628A=
XR_001750472.1:n.4680A=
NM_020937.4:c.4536A= MANE Select NP_065988.1:p.Leu1512=
NM_001308133.2:c.4458A= NP_001295062.1:p.Leu1486=