Canonical Allele Identifier: CA389607809

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45183880C>G , CM000676.2:g.45183880C>G	GRCh38
NC_000014.8:g.45653083C>G , CM000676.1:g.45653083C>G	GRCh37
NC_000014.7:g.44722833C>G	NCBI36
NG_007417.1:g.52948C>G , LRG_502:g.52948C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4493C>G MANE Select	NP_065988.1:p.Pro1498Arg
ENST00000267430.10:c.4493C>G MANE Select	ENSP00000267430.5:p.Pro1498Arg
NM_001308133.1:c.4415C>G	NP_001295062.1:p.Pro1472Arg
NM_001308133.2:c.4415C>G	NP_001295062.1:p.Pro1472Arg
NM_020937.2:c.4493C>G , LRG_502t1:c.4493C>G	NP_065988.1:p.Pro1498Arg
NM_020937.3:c.4493C>G	NP_065988.1:p.Pro1498Arg
ENST00000267430.9:c.4493C>G	ENSP00000267430.5:p.Pro1498Arg
ENST00000542564.6:c.4415C>G	ENSP00000442493.2:p.Pro1472Arg
ENST00000554809.5:c.1290C>G
ENST00000554809.6:c.2705C>G	ENSP00000450632.2:p.Pro902Arg
ENST00000555013.1:n.326C>G
ENST00000555484.2:c.271C>G
ENST00000556250.5:c.3041C>G	ENSP00000452033.1:p.Pro1014Arg
ENST00000556250.6:c.4286C>G	ENSP00000452033.2:p.Pro1429Arg
ENST00000557110.2:c.271C>G
ENST00000696642.1:c.*3304C>G	ENSP00000512775.1:n.*3304C>G
ENST00000696644.1:n.229C>G
ENST00000696645.1:n.383C>G
ENST00000696647.1:c.4493C>G	ENSP00000512778.1:p.Pro1498Arg
ENST00000696648.1:c.*2518C>G	ENSP00000512779.1:n.*2518C>G
ENST00000696649.1:c.4337C>G	ENSP00000512780.1:p.Pro1446Arg
ENST00000696650.1:n.4441C>G
ENST00000696659.1:c.2491C>G
ENST00000696663.1:c.3424C>G
ENST00000696664.1:c.3325C>G
ENST00000696665.1:c.271C>G
ENST00000696675.1:c.*249C>G	ENSP00000512799.1:n.*249C>G
ENST00000696683.1:c.3310C>G
ENST00000696684.1:c.3310C>G
ENST00000696685.1:c.3310C>G
ENST00000696686.1:n.1230C>G
XM_011537034.1:c.4508C>G	XP_011535336.1:p.Pro1503Arg
XM_011537034.2:c.4508C>G	XP_011535336.1:p.Pro1503Arg
XM_011537035.1:c.4430C>G	XP_011535337.1:p.Pro1477Arg
XM_011537035.3:c.4430C>G	XP_011535337.1:p.Pro1477Arg
XM_011537036.1:c.4508C>G	XP_011535338.1:p.Pro1503Arg
XM_011537037.1:c.2522C>G	XP_011535339.1:p.Pro841Arg
XM_011537037.3:c.2522C>G	XP_011535339.1:p.Pro841Arg
XM_017021523.1:c.4508C>G	XP_016877012.1:p.Pro1503Arg
XM_017021524.2:c.3545C>G	XP_016877013.1:p.Pro1182Arg
XM_017021525.2:c.3323C>G	XP_016877014.1:p.Pro1108Arg
XM_017021526.2:c.3323C>G	XP_016877015.1:p.Pro1108Arg
XM_017021527.1:c.3308C>G	XP_016877016.1:p.Pro1103Arg
XR_001750470.1:n.4600C>G
XR_001750471.2:n.4585C>G
XR_001750472.1:n.4637C>G