Canonical Allele Identifier: CA7169583

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45176591A>G , CM000676.2:g.45176591A>G	GRCh38
NC_000014.8:g.45645794A>G , CM000676.1:g.45645794A>G	GRCh37
NC_000014.7:g.44715544A>G	NCBI36
NG_007417.1:g.45659A>G , LRG_502:g.45659A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.3837A>G MANE Select	NP_065988.1:p.Ala1279=
ENST00000267430.10:c.3837A>G MANE Select	ENSP00000267430.5:p.Ala1279=
NM_001308133.1:c.3759A>G	NP_001295062.1:p.Ala1253=
NM_001308133.2:c.3759A>G	NP_001295062.1:p.Ala1253=
NM_020937.2:c.3837A>G , LRG_502t1:c.3837A>G	NP_065988.1:p.Ala1279=
NM_020937.3:c.3837A>G	NP_065988.1:p.Ala1279=
ENST00000267430.9:c.3837A>G	ENSP00000267430.5:p.Ala1279=
ENST00000542564.6:c.3759A>G	ENSP00000442493.2:p.Ala1253=
ENST00000554809.5:c.634A>G
ENST00000554809.6:c.2049A>G	ENSP00000450632.2:p.Ala683=
ENST00000556250.5:c.2385A>G	ENSP00000452033.1:p.Ala795=
ENST00000556250.6:c.3630A>G	ENSP00000452033.2:p.Ala1210=
ENST00000696641.1:c.3678A>G	ENSP00000512774.1:p.Ala1226=
ENST00000696642.1:c.*2648A>G	ENSP00000512775.1:n.*2648A>G
ENST00000696646.1:c.*2648A>G	ENSP00000512777.1:n.*2648A>G
ENST00000696647.1:c.3837A>G	ENSP00000512778.1:p.Ala1279=
ENST00000696648.1:c.*1862A>G	ENSP00000512779.1:n.*1862A>G
ENST00000696649.1:c.3681A>G	ENSP00000512780.1:p.Ala1227=
ENST00000696650.1:n.3785A>G
ENST00000696659.1:c.1835A>G
ENST00000696663.1:c.2654A>G
ENST00000696664.1:c.2654A>G
ENST00000696675.1:c.3837A>G	ENSP00000512799.1:p.Ala1279=
ENST00000696683.1:c.2654A>G
ENST00000696684.1:c.2654A>G
ENST00000696685.1:c.2654A>G
XM_011537034.1:c.3837A>G	XP_011535336.1:p.Ala1279=
XM_011537034.2:c.3837A>G	XP_011535336.1:p.Ala1279=
XM_011537035.1:c.3759A>G	XP_011535337.1:p.Ala1253=
XM_011537035.3:c.3759A>G	XP_011535337.1:p.Ala1253=
XM_011537036.1:c.3837A>G	XP_011535338.1:p.Ala1279=
XM_011537037.1:c.1851A>G	XP_011535339.1:p.Ala617=
XM_011537037.3:c.1851A>G	XP_011535339.1:p.Ala617=
XM_017021523.1:c.3837A>G	XP_016877012.1:p.Ala1279=
XM_017021524.2:c.2874A>G	XP_016877013.1:p.Ala958=
XM_017021525.2:c.2652A>G	XP_016877014.1:p.Ala884=
XM_017021526.2:c.2652A>G	XP_016877015.1:p.Ala884=
XM_017021527.1:c.2652A>G	XP_016877016.1:p.Ala884=
XR_001750470.1:n.3929A>G
XR_001750471.2:n.3929A>G
XR_001750472.1:n.3929A>G