Canonical Allele Identifier: CA7170130

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45199957A>G , CM000676.2:g.45199957A>G	GRCh38
NC_000014.8:g.45669160A>G , CM000676.1:g.45669160A>G	GRCh37
NC_000014.7:g.44738910A>G	NCBI36
NG_007417.1:g.69025A>G , LRG_502:g.69025A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.6096A>G MANE Select	NP_065988.1:p.Ile2032Met
ENST00000267430.10:c.6096A>G MANE Select	ENSP00000267430.5:p.Ile2032Met
NM_001308133.1:c.6018A>G	NP_001295062.1:p.Ile2006Met
NM_001308133.2:c.6018A>G	NP_001295062.1:p.Ile2006Met
NM_020937.2:c.6096A>G , LRG_502t1:c.6096A>G	NP_065988.1:p.Ile2032Met
NM_020937.3:c.6096A>G	NP_065988.1:p.Ile2032Met
ENST00000267430.9:c.6096A>G	ENSP00000267430.5:p.Ile2032Met
ENST00000542564.6:c.6018A>G	ENSP00000442493.2:p.Ile2006Met
ENST00000553551.1:n.589A>G
ENST00000553551.2:n.2296A>G
ENST00000554809.5:c.2998A>G
ENST00000554809.6:c.4413A>G	ENSP00000450632.2:p.Ile1471Met
ENST00000555484.1:c.374A>G	ENSP00000450797.1:n.374A>G
ENST00000555484.2:c.1774A>G
ENST00000556250.5:c.4644A>G	ENSP00000452033.1:p.Ile1548Met
ENST00000556250.6:c.5889A>G	ENSP00000452033.2:p.Ile1963Met
ENST00000557110.2:c.1786A>G
ENST00000696645.1:n.1986A>G
ENST00000696647.1:c.*329A>G	ENSP00000512778.1:n.*329A>G
ENST00000696648.1:c.*4121A>G	ENSP00000512779.1:n.*4121A>G
ENST00000696649.1:c.5940A>G	ENSP00000512780.1:p.Ile1980Met
ENST00000696651.1:n.2536A>G
ENST00000696663.1:c.5027A>G
ENST00000696664.1:c.4928A>G
ENST00000696665.1:c.1582A>G
ENST00000696675.1:c.*1852A>G	ENSP00000512799.1:n.*1852A>G
ENST00000696683.1:c.4724A>G
ENST00000696684.1:c.4245A>G
ENST00000696685.1:c.4914A>G
ENST00000696686.1:n.2833A>G
XM_011537034.1:c.6111A>G	XP_011535336.1:p.Ile2037Met
XM_011537034.2:c.6111A>G	XP_011535336.1:p.Ile2037Met
XM_011537035.1:c.6033A>G	XP_011535337.1:p.Ile2011Met
XM_011537035.3:c.6033A>G	XP_011535337.1:p.Ile2011Met
XM_011537037.1:c.4125A>G	XP_011535339.1:p.Ile1375Met
XM_011537037.3:c.4125A>G	XP_011535339.1:p.Ile1375Met
XM_017021523.1:c.*37A>G	XP_016877012.1:n.*37A>G
XM_017021524.2:c.5148A>G	XP_016877013.1:p.Ile1716Met
XM_017021525.2:c.4926A>G	XP_016877014.1:p.Ile1642Met
XM_017021526.2:c.4926A>G	XP_016877015.1:p.Ile1642Met
XM_017021527.1:c.4911A>G	XP_016877016.1:p.Ile1637Met
XR_001750470.1:n.5827A>G
XR_001750471.2:n.5812A>G