Canonical Allele Identifier: CA7169916

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45189174G>A , CM000676.2:g.45189174G>A	GRCh38
NC_000014.8:g.45658377G>A , CM000676.1:g.45658377G>A	GRCh37
NC_000014.7:g.44728127G>A	NCBI36
NG_007417.1:g.58242G>A , LRG_502:g.58242G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.5152G>A MANE Select	NP_065988.1:p.Val1718Met
ENST00000267430.10:c.5152G>A MANE Select	ENSP00000267430.5:p.Val1718Met
NM_001308133.1:c.5074G>A	NP_001295062.1:p.Val1692Met
NM_001308133.2:c.5074G>A	NP_001295062.1:p.Val1692Met
NM_020937.2:c.5152G>A , LRG_502t1:c.5152G>A	NP_065988.1:p.Val1718Met
NM_020937.3:c.5152G>A	NP_065988.1:p.Val1718Met
ENST00000267430.9:c.5152G>A	ENSP00000267430.5:p.Val1718Met
ENST00000542564.6:c.5074G>A	ENSP00000442493.2:p.Val1692Met
ENST00000554809.5:c.1949G>A
ENST00000554809.6:c.3364G>A	ENSP00000450632.2:p.Val1122Met
ENST00000555484.2:c.930G>A
ENST00000556250.5:c.3700G>A	ENSP00000452033.1:p.Val1234Met
ENST00000556250.6:c.4945G>A	ENSP00000452033.2:p.Val1649Met
ENST00000557110.2:c.930G>A
ENST00000696642.1:c.*3963G>A	ENSP00000512775.1:n.*3963G>A
ENST00000696645.1:n.1042G>A
ENST00000696647.1:c.5152G>A	ENSP00000512778.1:p.Val1718Met
ENST00000696648.1:c.*3177G>A	ENSP00000512779.1:n.*3177G>A
ENST00000696649.1:c.4996G>A	ENSP00000512780.1:p.Val1666Met
ENST00000696650.1:n.5100G>A
ENST00000696659.1:c.3150G>A
ENST00000696663.1:c.4083G>A
ENST00000696664.1:c.3984G>A
ENST00000696665.1:c.930G>A
ENST00000696675.1:c.*908G>A	ENSP00000512799.1:n.*908G>A
ENST00000696683.1:c.3968+1G>A
ENST00000696684.1:c.3969G>A
ENST00000696685.1:c.3969G>A
ENST00000696686.1:n.1889G>A
XM_011537034.1:c.5167G>A	XP_011535336.1:p.Val1723Met
XM_011537034.2:c.5167G>A	XP_011535336.1:p.Val1723Met
XM_011537035.1:c.5089G>A	XP_011535337.1:p.Val1697Met
XM_011537035.3:c.5089G>A	XP_011535337.1:p.Val1697Met
XM_011537036.1:c.5167G>A	XP_011535338.1:p.Val1723Met
XM_011537037.1:c.3181G>A	XP_011535339.1:p.Val1061Met
XM_011537037.3:c.3181G>A	XP_011535339.1:p.Val1061Met
XM_017021523.1:c.5167G>A	XP_016877012.1:p.Val1723Met
XM_017021524.2:c.4204G>A	XP_016877013.1:p.Val1402Met
XM_017021525.2:c.3982G>A	XP_016877014.1:p.Val1328Met
XM_017021526.2:c.3982G>A	XP_016877015.1:p.Val1328Met
XM_017021527.1:c.3967G>A	XP_016877016.1:p.Val1323Met
XR_001750470.1:n.5259G>A
XR_001750471.2:n.5244G>A