Canonical Allele Identifier: CA2133624531

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45185305A= , CM000676.2:g.45185305A=	GRCh38
NC_000014.8:g.45654508A= , CM000676.1:g.45654508A=	GRCh37
NC_000014.7:g.44724258A=	NCBI36
NG_007417.1:g.54373A= , LRG_502:g.54373A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000554809.6:c.2816A=	ENSP00000450632.2:p.Glu939=
ENST00000555484.2:c.382A=
ENST00000556250.6:c.4397A=	ENSP00000452033.2:p.Glu1466=
ENST00000557110.2:c.382A=
ENST00000696642.1:c.*3415A=	ENSP00000512775.1:n.*3415A=
ENST00000696644.1:n.340A=
ENST00000696645.1:n.494A=
ENST00000696647.1:c.4604A=	ENSP00000512778.1:p.Glu1535=
ENST00000696648.1:c.*2629A=	ENSP00000512779.1:n.*2629A=
ENST00000696649.1:c.4448A=	ENSP00000512780.1:p.Glu1483=
ENST00000696650.1:n.4552A=
ENST00000696659.1:c.2602A=
ENST00000696663.1:c.3535A=
ENST00000696664.1:c.3436A=
ENST00000696665.1:c.382A=
ENST00000696675.1:c.*360A=	ENSP00000512799.1:n.*360A=
ENST00000696683.1:c.3421A=
ENST00000696684.1:c.3421A=
ENST00000696685.1:c.3421A=
ENST00000696686.1:n.1341A=
ENST00000267430.10:c.4604A= MANE Select	ENSP00000267430.5:p.Glu1535=
ENST00000267430.9:c.4604A=	ENSP00000267430.5:p.Glu1535=
ENST00000542564.6:c.4526A=	ENSP00000442493.2:p.Glu1509=
ENST00000554809.5:c.1401A=
ENST00000555013.1:n.437A=
ENST00000556250.5:c.3152A=	ENSP00000452033.1:p.Glu1051=
NM_001308133.1:c.4526A=	NP_001295062.1:p.Glu1509=
NM_020937.2:c.4604A= , LRG_502t1:c.4604A=	NP_065988.1:p.Glu1535=
NM_020937.3:c.4604A=	NP_065988.1:p.Glu1535=
XM_011537034.1:c.4619A=	XP_011535336.1:p.Glu1540=
XM_011537035.1:c.4541A=	XP_011535337.1:p.Glu1514=
XM_011537036.1:c.4619A=	XP_011535338.1:p.Glu1540=
XM_011537037.1:c.2633A=	XP_011535339.1:p.Glu878=
XM_011537034.2:c.4619A=	XP_011535336.1:p.Glu1540=
XM_011537035.3:c.4541A=	XP_011535337.1:p.Glu1514=
XM_011537037.3:c.2633A=	XP_011535339.1:p.Glu878=
XM_017021523.1:c.4619A=	XP_016877012.1:p.Glu1540=
XM_017021524.2:c.3656A=	XP_016877013.1:p.Glu1219=
XM_017021525.2:c.3434A=	XP_016877014.1:p.Glu1145=
XM_017021526.2:c.3434A=	XP_016877015.1:p.Glu1145=
XM_017021527.1:c.3419A=	XP_016877016.1:p.Glu1140=
XR_001750470.1:n.4711A=
XR_001750471.2:n.4696A=
XR_001750472.1:n.4748A=
NM_020937.4:c.4604A= MANE Select	NP_065988.1:p.Glu1535=
NM_001308133.2:c.4526A=	NP_001295062.1:p.Glu1509=