Canonical Allele Identifier: CA2801411017

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185308dup , CM000676.2:g.45185308dup	GRCh38
NC_000014.8:g.45654511dup , CM000676.1:g.45654511dup	GRCh37
NC_000014.7:g.44724261dup	NCBI36
NG_007417.1:g.54376dup , LRG_502:g.54376dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2819dup	ENSP00000450632.2:p.Asn940LysfsTer2
ENST00000555484.2:c.385dup
ENST00000556250.6:c.4400dup	ENSP00000452033.2:p.Asn1467LysfsTer2
ENST00000557110.2:c.385dup
ENST00000696642.1:c.*3418dup	ENSP00000512775.1:n.*3418dup
ENST00000696644.1:n.343dup
ENST00000696645.1:n.497dup
ENST00000696647.1:c.4607dup	ENSP00000512778.1:p.Asn1536LysfsTer2
ENST00000696648.1:c.*2632dup	ENSP00000512779.1:n.*2632dup
ENST00000696649.1:c.4451dup	ENSP00000512780.1:p.Asn1484LysfsTer2
ENST00000696650.1:n.4555dup
ENST00000696659.1:c.2605dup
ENST00000696663.1:c.3538dup
ENST00000696664.1:c.3439dup
ENST00000696665.1:c.385dup
ENST00000696675.1:c.*363dup	ENSP00000512799.1:n.*363dup
ENST00000696683.1:c.3424dup
ENST00000696684.1:c.3424dup
ENST00000696685.1:c.3424dup
ENST00000696686.1:n.1344dup
ENST00000267430.10:c.4607dup MANE Select	ENSP00000267430.5:p.Asn1536LysfsTer2
ENST00000267430.9:c.4607dup	ENSP00000267430.5:p.Asn1536LysfsTer2
ENST00000542564.6:c.4529dup	ENSP00000442493.2:p.Asn1510LysfsTer2
ENST00000554809.5:c.1404dup
ENST00000555013.1:n.440dup
ENST00000556250.5:c.3155dup	ENSP00000452033.1:p.Asn1052LysfsTer2
NM_001308133.1:c.4529dup	NP_001295062.1:p.Asn1510LysfsTer2
NM_020937.2:c.4607dup , LRG_502t1:c.4607dup	NP_065988.1:p.Asn1536LysfsTer2
NM_020937.3:c.4607dup	NP_065988.1:p.Asn1536LysfsTer2
XM_011537034.1:c.4622dup	XP_011535336.1:p.Asn1541LysfsTer2
XM_011537035.1:c.4544dup	XP_011535337.1:p.Asn1515LysfsTer2
XM_011537036.1:c.4622dup	XP_011535338.1:p.Asn1541LysfsTer2
XM_011537037.1:c.2636dup	XP_011535339.1:p.Asn879LysfsTer2
XM_011537034.2:c.4622dup	XP_011535336.1:p.Asn1541LysfsTer2
XM_011537035.3:c.4544dup	XP_011535337.1:p.Asn1515LysfsTer2
XM_011537037.3:c.2636dup	XP_011535339.1:p.Asn879LysfsTer2
XM_017021523.1:c.4622dup	XP_016877012.1:p.Asn1541LysfsTer2
XM_017021524.2:c.3659dup	XP_016877013.1:p.Asn1220LysfsTer2
XM_017021525.2:c.3437dup	XP_016877014.1:p.Asn1146LysfsTer2
XM_017021526.2:c.3437dup	XP_016877015.1:p.Asn1146LysfsTer2
XM_017021527.1:c.3422dup	XP_016877016.1:p.Asn1141LysfsTer2
XR_001750470.1:n.4714dup
XR_001750471.2:n.4699dup
XR_001750472.1:n.4751dup
NM_020937.4:c.4607dup MANE Select	NP_065988.1:p.Asn1536LysfsTer2
NM_001308133.2:c.4529dup	NP_001295062.1:p.Asn1510LysfsTer2