Canonical Allele Identifier: CA389603460

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45176652G>T , CM000676.2:g.45176652G>T	GRCh38
NC_000014.8:g.45645855G>T , CM000676.1:g.45645855G>T	GRCh37
NC_000014.7:g.44715605G>T	NCBI36
NG_007417.1:g.45720G>T , LRG_502:g.45720G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.3898G>T MANE Select	NP_065988.1:p.Glu1300Ter
ENST00000267430.10:c.3898G>T MANE Select	ENSP00000267430.5:p.Glu1300Ter
NM_001308133.1:c.3820G>T	NP_001295062.1:p.Glu1274Ter
NM_001308133.2:c.3820G>T	NP_001295062.1:p.Glu1274Ter
NM_020937.2:c.3898G>T , LRG_502t1:c.3898G>T	NP_065988.1:p.Glu1300Ter
NM_020937.3:c.3898G>T	NP_065988.1:p.Glu1300Ter
ENST00000267430.9:c.3898G>T	ENSP00000267430.5:p.Glu1300Ter
ENST00000542564.6:c.3820G>T	ENSP00000442493.2:p.Glu1274Ter
ENST00000554809.5:c.695G>T
ENST00000554809.6:c.2110G>T	ENSP00000450632.2:p.Glu704Ter
ENST00000556250.5:c.2446G>T	ENSP00000452033.1:p.Glu816Ter
ENST00000556250.6:c.3691G>T	ENSP00000452033.2:p.Glu1231Ter
ENST00000696641.1:c.3739G>T	ENSP00000512774.1:p.Glu1247Ter
ENST00000696642.1:c.*2709G>T	ENSP00000512775.1:n.*2709G>T
ENST00000696646.1:c.*2709G>T	ENSP00000512777.1:n.*2709G>T
ENST00000696647.1:c.3898G>T	ENSP00000512778.1:p.Glu1300Ter
ENST00000696648.1:c.*1923G>T	ENSP00000512779.1:n.*1923G>T
ENST00000696649.1:c.3742G>T	ENSP00000512780.1:p.Glu1248Ter
ENST00000696650.1:n.3846G>T
ENST00000696659.1:c.1896G>T
ENST00000696663.1:c.2715G>T
ENST00000696664.1:c.2715G>T
ENST00000696675.1:c.3898G>T	ENSP00000512799.1:p.Glu1300Ter
ENST00000696683.1:c.2715G>T
ENST00000696684.1:c.2715G>T
ENST00000696685.1:c.2715G>T
XM_011537034.1:c.3898G>T	XP_011535336.1:p.Glu1300Ter
XM_011537034.2:c.3898G>T	XP_011535336.1:p.Glu1300Ter
XM_011537035.1:c.3820G>T	XP_011535337.1:p.Glu1274Ter
XM_011537035.3:c.3820G>T	XP_011535337.1:p.Glu1274Ter
XM_011537036.1:c.3898G>T	XP_011535338.1:p.Glu1300Ter
XM_011537037.1:c.1912G>T	XP_011535339.1:p.Glu638Ter
XM_011537037.3:c.1912G>T	XP_011535339.1:p.Glu638Ter
XM_017021523.1:c.3898G>T	XP_016877012.1:p.Glu1300Ter
XM_017021524.2:c.2935G>T	XP_016877013.1:p.Glu979Ter
XM_017021525.2:c.2713G>T	XP_016877014.1:p.Glu905Ter
XM_017021526.2:c.2713G>T	XP_016877015.1:p.Glu905Ter
XM_017021527.1:c.2713G>T	XP_016877016.1:p.Glu905Ter
XR_001750470.1:n.3990G>T
XR_001750471.2:n.3990G>T
XR_001750472.1:n.3990G>T