Canonical Allele Identifier: CA389602046

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45176310A>G , CM000676.2:g.45176310A>G	GRCh38
NC_000014.8:g.45645513A>G , CM000676.1:g.45645513A>G	GRCh37
NC_000014.7:g.44715263A>G	NCBI36
NG_007417.1:g.45378A>G , LRG_502:g.45378A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.3556A>G MANE Select	NP_065988.1:p.Asn1186Asp
ENST00000267430.10:c.3556A>G MANE Select	ENSP00000267430.5:p.Asn1186Asp
NM_001308133.1:c.3478A>G	NP_001295062.1:p.Asn1160Asp
NM_001308133.2:c.3478A>G	NP_001295062.1:p.Asn1160Asp
NM_020937.2:c.3556A>G , LRG_502t1:c.3556A>G	NP_065988.1:p.Asn1186Asp
NM_020937.3:c.3556A>G	NP_065988.1:p.Asn1186Asp
ENST00000267430.9:c.3556A>G	ENSP00000267430.5:p.Asn1186Asp
ENST00000542564.6:c.3478A>G	ENSP00000442493.2:p.Asn1160Asp
ENST00000554809.5:c.353A>G
ENST00000554809.6:c.1768A>G	ENSP00000450632.2:p.Asn590Asp
ENST00000556250.5:c.2104A>G	ENSP00000452033.1:p.Asn702Asp
ENST00000556250.6:c.3349A>G	ENSP00000452033.2:p.Asn1117Asp
ENST00000696641.1:c.3397A>G	ENSP00000512774.1:p.Asn1133Asp
ENST00000696642.1:c.*2367A>G	ENSP00000512775.1:n.*2367A>G
ENST00000696646.1:c.*2367A>G	ENSP00000512777.1:n.*2367A>G
ENST00000696647.1:c.3556A>G	ENSP00000512778.1:p.Asn1186Asp
ENST00000696648.1:c.*1581A>G	ENSP00000512779.1:n.*1581A>G
ENST00000696649.1:c.3400A>G	ENSP00000512780.1:p.Asn1134Asp
ENST00000696650.1:n.3504A>G
ENST00000696659.1:c.1554A>G
ENST00000696663.1:c.2373A>G
ENST00000696664.1:c.2373A>G
ENST00000696675.1:c.3556A>G	ENSP00000512799.1:p.Asn1186Asp
ENST00000696683.1:c.2373A>G
ENST00000696684.1:c.2373A>G
ENST00000696685.1:c.2373A>G
XM_011537034.1:c.3556A>G	XP_011535336.1:p.Asn1186Asp
XM_011537034.2:c.3556A>G	XP_011535336.1:p.Asn1186Asp
XM_011537035.1:c.3478A>G	XP_011535337.1:p.Asn1160Asp
XM_011537035.3:c.3478A>G	XP_011535337.1:p.Asn1160Asp
XM_011537036.1:c.3556A>G	XP_011535338.1:p.Asn1186Asp
XM_011537037.1:c.1570A>G	XP_011535339.1:p.Asn524Asp
XM_011537037.3:c.1570A>G	XP_011535339.1:p.Asn524Asp
XM_017021523.1:c.3556A>G	XP_016877012.1:p.Asn1186Asp
XM_017021524.2:c.2593A>G	XP_016877013.1:p.Asn865Asp
XM_017021525.2:c.2371A>G	XP_016877014.1:p.Asn791Asp
XM_017021526.2:c.2371A>G	XP_016877015.1:p.Asn791Asp
XM_017021527.1:c.2371A>G	XP_016877016.1:p.Asn791Asp
XR_001750470.1:n.3648A>G
XR_001750471.2:n.3648A>G
XR_001750472.1:n.3648A>G