Canonical Allele Identifier: CA7169754

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45183852G>C , CM000676.2:g.45183852G>C	GRCh38
NC_000014.8:g.45653055G>C , CM000676.1:g.45653055G>C	GRCh37
NC_000014.7:g.44722805G>C	NCBI36
NG_007417.1:g.52920G>C , LRG_502:g.52920G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4465G>C MANE Select	NP_065988.1:p.Gly1489Arg
ENST00000267430.10:c.4465G>C MANE Select	ENSP00000267430.5:p.Gly1489Arg
NM_001308133.1:c.4387G>C	NP_001295062.1:p.Gly1463Arg
NM_001308133.2:c.4387G>C	NP_001295062.1:p.Gly1463Arg
NM_020937.2:c.4465G>C , LRG_502t1:c.4465G>C	NP_065988.1:p.Gly1489Arg
NM_020937.3:c.4465G>C	NP_065988.1:p.Gly1489Arg
ENST00000267430.9:c.4465G>C	ENSP00000267430.5:p.Gly1489Arg
ENST00000542564.6:c.4387G>C	ENSP00000442493.2:p.Gly1463Arg
ENST00000554809.5:c.1262G>C
ENST00000554809.6:c.2677G>C	ENSP00000450632.2:p.Gly893Arg
ENST00000555013.1:n.298G>C
ENST00000555484.2:c.243G>C
ENST00000556250.5:c.3013G>C	ENSP00000452033.1:p.Gly1005Arg
ENST00000556250.6:c.4258G>C	ENSP00000452033.2:p.Gly1420Arg
ENST00000557110.2:c.243G>C
ENST00000696642.1:c.*3276G>C	ENSP00000512775.1:n.*3276G>C
ENST00000696644.1:n.201G>C
ENST00000696645.1:n.355G>C
ENST00000696647.1:c.4465G>C	ENSP00000512778.1:p.Gly1489Arg
ENST00000696648.1:c.*2490G>C	ENSP00000512779.1:n.*2490G>C
ENST00000696649.1:c.4309G>C	ENSP00000512780.1:p.Gly1437Arg
ENST00000696650.1:n.4413G>C
ENST00000696659.1:c.2463G>C
ENST00000696663.1:c.3396G>C
ENST00000696664.1:c.3297G>C
ENST00000696665.1:c.243G>C
ENST00000696675.1:c.*221G>C	ENSP00000512799.1:n.*221G>C
ENST00000696683.1:c.3282G>C
ENST00000696684.1:c.3282G>C
ENST00000696685.1:c.3282G>C
ENST00000696686.1:n.1202G>C
XM_011537034.1:c.4480G>C	XP_011535336.1:p.Gly1494Arg
XM_011537034.2:c.4480G>C	XP_011535336.1:p.Gly1494Arg
XM_011537035.1:c.4402G>C	XP_011535337.1:p.Gly1468Arg
XM_011537035.3:c.4402G>C	XP_011535337.1:p.Gly1468Arg
XM_011537036.1:c.4480G>C	XP_011535338.1:p.Gly1494Arg
XM_011537037.1:c.2494G>C	XP_011535339.1:p.Gly832Arg
XM_011537037.3:c.2494G>C	XP_011535339.1:p.Gly832Arg
XM_017021523.1:c.4480G>C	XP_016877012.1:p.Gly1494Arg
XM_017021524.2:c.3517G>C	XP_016877013.1:p.Gly1173Arg
XM_017021525.2:c.3295G>C	XP_016877014.1:p.Gly1099Arg
XM_017021526.2:c.3295G>C	XP_016877015.1:p.Gly1099Arg
XM_017021527.1:c.3280G>C	XP_016877016.1:p.Gly1094Arg
XR_001750470.1:n.4572G>C
XR_001750471.2:n.4557G>C
XR_001750472.1:n.4609G>C