Canonical Allele Identifier: CA2133624476
Gene: FANCM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45185253C= , CM000676.2:g.45185253C= GRCh38
NC_000014.8:g.45654456C= , CM000676.1:g.45654456C= GRCh37
NC_000014.7:g.44724206C= NCBI36
NG_007417.1:g.54321C= , LRG_502:g.54321C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000554809.6:c.2764C= ENSP00000450632.2:p.Leu922=
ENST00000555484.2:c.330C=
ENST00000556250.6:c.4345C= ENSP00000452033.2:p.Leu1449=
ENST00000557110.2:c.330C=
ENST00000696642.1:c.*3363C= ENSP00000512775.1:n.*3363C=
ENST00000696644.1:n.288C=
ENST00000696645.1:n.442C=
ENST00000696647.1:c.4552C= ENSP00000512778.1:p.Leu1518=
ENST00000696648.1:c.*2577C= ENSP00000512779.1:n.*2577C=
ENST00000696649.1:c.4396C= ENSP00000512780.1:p.Leu1466=
ENST00000696650.1:n.4500C=
ENST00000696659.1:c.2550C=
ENST00000696663.1:c.3483C=
ENST00000696664.1:c.3384C=
ENST00000696665.1:c.330C=
ENST00000696675.1:c.*308C= ENSP00000512799.1:n.*308C=
ENST00000696683.1:c.3369C=
ENST00000696684.1:c.3369C=
ENST00000696685.1:c.3369C=
ENST00000696686.1:n.1289C=
ENST00000267430.10:c.4552C= MANE Select ENSP00000267430.5:p.Leu1518=
ENST00000267430.9:c.4552C= ENSP00000267430.5:p.Leu1518=
ENST00000542564.6:c.4474C= ENSP00000442493.2:p.Leu1492=
ENST00000554809.5:c.1349C=
ENST00000555013.1:n.385C=
ENST00000556250.5:c.3100C= ENSP00000452033.1:p.Leu1034=
NM_001308133.1:c.4474C= NP_001295062.1:p.Leu1492=
NM_020937.2:c.4552C= , LRG_502t1:c.4552C= NP_065988.1:p.Leu1518=
NM_020937.3:c.4552C= NP_065988.1:p.Leu1518=
XM_011537034.1:c.4567C= XP_011535336.1:p.Leu1523=
XM_011537035.1:c.4489C= XP_011535337.1:p.Leu1497=
XM_011537036.1:c.4567C= XP_011535338.1:p.Leu1523=
XM_011537037.1:c.2581C= XP_011535339.1:p.Leu861=
XM_011537034.2:c.4567C= XP_011535336.1:p.Leu1523=
XM_011537035.3:c.4489C= XP_011535337.1:p.Leu1497=
XM_011537037.3:c.2581C= XP_011535339.1:p.Leu861=
XM_017021523.1:c.4567C= XP_016877012.1:p.Leu1523=
XM_017021524.2:c.3604C= XP_016877013.1:p.Leu1202=
XM_017021525.2:c.3382C= XP_016877014.1:p.Leu1128=
XM_017021526.2:c.3382C= XP_016877015.1:p.Leu1128=
XM_017021527.1:c.3367C= XP_016877016.1:p.Leu1123=
XR_001750470.1:n.4659C=
XR_001750471.2:n.4644C=
XR_001750472.1:n.4696C=
NM_020937.4:c.4552C= MANE Select NP_065988.1:p.Leu1518=
NM_001308133.2:c.4474C= NP_001295062.1:p.Leu1492=