Canonical Allele Identifier: CA7169877

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45188956G>A , CM000676.2:g.45188956G>A	GRCh38
NC_000014.8:g.45658159G>A , CM000676.1:g.45658159G>A	GRCh37
NC_000014.7:g.44727909G>A	NCBI36
NG_007417.1:g.58024G>A , LRG_502:g.58024G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4934G>A MANE Select	NP_065988.1:p.Arg1645His
ENST00000267430.10:c.4934G>A MANE Select	ENSP00000267430.5:p.Arg1645His
NM_001308133.1:c.4856G>A	NP_001295062.1:p.Arg1619His
NM_001308133.2:c.4856G>A	NP_001295062.1:p.Arg1619His
NM_020937.2:c.4934G>A , LRG_502t1:c.4934G>A	NP_065988.1:p.Arg1645His
NM_020937.3:c.4934G>A	NP_065988.1:p.Arg1645His
ENST00000267430.9:c.4934G>A	ENSP00000267430.5:p.Arg1645His
ENST00000542564.6:c.4856G>A	ENSP00000442493.2:p.Arg1619His
ENST00000554809.5:c.1731G>A
ENST00000554809.6:c.3146G>A	ENSP00000450632.2:p.Arg1049His
ENST00000555484.2:c.712G>A
ENST00000556250.5:c.3482G>A	ENSP00000452033.1:p.Arg1161His
ENST00000556250.6:c.4727G>A	ENSP00000452033.2:p.Arg1576His
ENST00000557110.2:c.712G>A
ENST00000696642.1:c.*3745G>A	ENSP00000512775.1:n.*3745G>A
ENST00000696645.1:n.824G>A
ENST00000696647.1:c.4934G>A	ENSP00000512778.1:p.Arg1645His
ENST00000696648.1:c.*2959G>A	ENSP00000512779.1:n.*2959G>A
ENST00000696649.1:c.4778G>A	ENSP00000512780.1:p.Arg1593His
ENST00000696650.1:n.4882G>A
ENST00000696659.1:c.2932G>A
ENST00000696663.1:c.3865G>A
ENST00000696664.1:c.3766G>A
ENST00000696665.1:c.712G>A
ENST00000696675.1:c.*690G>A	ENSP00000512799.1:n.*690G>A
ENST00000696683.1:c.3751G>A
ENST00000696684.1:c.3751G>A
ENST00000696685.1:c.3751G>A
ENST00000696686.1:n.1671G>A
XM_011537034.1:c.4949G>A	XP_011535336.1:p.Arg1650His
XM_011537034.2:c.4949G>A	XP_011535336.1:p.Arg1650His
XM_011537035.1:c.4871G>A	XP_011535337.1:p.Arg1624His
XM_011537035.3:c.4871G>A	XP_011535337.1:p.Arg1624His
XM_011537036.1:c.4949G>A	XP_011535338.1:p.Arg1650His
XM_011537037.1:c.2963G>A	XP_011535339.1:p.Arg988His
XM_011537037.3:c.2963G>A	XP_011535339.1:p.Arg988His
XM_017021523.1:c.4949G>A	XP_016877012.1:p.Arg1650His
XM_017021524.2:c.3986G>A	XP_016877013.1:p.Arg1329His
XM_017021525.2:c.3764G>A	XP_016877014.1:p.Arg1255His
XM_017021526.2:c.3764G>A	XP_016877015.1:p.Arg1255His
XM_017021527.1:c.3749G>A	XP_016877016.1:p.Arg1250His
XR_001750470.1:n.5041G>A
XR_001750471.2:n.5026G>A
XR_001750472.1:n.5078G>A