Canonical Allele Identifier: CA389609698

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45187780G>A , CM000676.2:g.45187780G>A	GRCh38
NC_000014.8:g.45656983G>A , CM000676.1:g.45656983G>A	GRCh37
NC_000014.7:g.44726733G>A	NCBI36
NG_007417.1:g.56848G>A , LRG_502:g.56848G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4673-1G>A MANE Select	NP_065988.1:n.4673-1G>A
ENST00000267430.10:c.4673-1G>A MANE Select	ENSP00000267430.5:n.4673-1G>A
NM_001308133.1:c.4595-1G>A	NP_001295062.1:n.4595-1G>A
NM_001308133.2:c.4595-1G>A	NP_001295062.1:n.4595-1G>A
NM_020937.2:c.4673-1G>A , LRG_502t1:c.4673-1G>A	NP_065988.1:n.4673-1G>A
NM_020937.3:c.4673-1G>A	NP_065988.1:n.4673-1G>A
ENST00000267430.9:c.4673-1G>A	ENSP00000267430.5:n.4673-1G>A
ENST00000542564.6:c.4595-1G>A	ENSP00000442493.2:n.4595-1G>A
ENST00000554809.5:c.1470-1G>A
ENST00000554809.6:c.2885-1G>A	ENSP00000450632.2:n.2885-1G>A
ENST00000555013.1:n.506-1G>A
ENST00000555484.2:c.451-1G>A
ENST00000556250.5:c.3221-1G>A	ENSP00000452033.1:n.3221-1G>A
ENST00000556250.6:c.4466-1G>A	ENSP00000452033.2:n.4466-1G>A
ENST00000557110.2:c.451-1G>A
ENST00000696642.1:c.*3484-1G>A	ENSP00000512775.1:n.*3484-1G>A
ENST00000696644.1:n.409-1G>A
ENST00000696645.1:n.563-1G>A
ENST00000696647.1:c.4673-1G>A	ENSP00000512778.1:n.4673-1G>A
ENST00000696648.1:c.*2698-1G>A	ENSP00000512779.1:n.*2698-1G>A
ENST00000696649.1:c.4517-1G>A	ENSP00000512780.1:n.4517-1G>A
ENST00000696650.1:n.4621-1G>A
ENST00000696659.1:c.2671-1G>A
ENST00000696663.1:c.3604-1G>A
ENST00000696664.1:c.3505-1G>A
ENST00000696665.1:c.451-1G>A
ENST00000696675.1:c.*429-1G>A	ENSP00000512799.1:n.*429-1G>A
ENST00000696683.1:c.3490-1G>A
ENST00000696684.1:c.3490-1G>A
ENST00000696685.1:c.3490-1G>A
ENST00000696686.1:n.1410-1G>A
XM_011537034.1:c.4688-1G>A	XP_011535336.1:n.4688-1G>A
XM_011537034.2:c.4688-1G>A	XP_011535336.1:n.4688-1G>A
XM_011537035.1:c.4610-1G>A	XP_011535337.1:n.4610-1G>A
XM_011537035.3:c.4610-1G>A	XP_011535337.1:n.4610-1G>A
XM_011537036.1:c.4688-1G>A	XP_011535338.1:n.4688-1G>A
XM_011537037.1:c.2702-1G>A	XP_011535339.1:n.2702-1G>A
XM_011537037.3:c.2702-1G>A	XP_011535339.1:n.2702-1G>A
XM_017021523.1:c.4688-1G>A	XP_016877012.1:n.4688-1G>A
XM_017021524.2:c.3725-1G>A	XP_016877013.1:n.3725-1G>A
XM_017021525.2:c.3503-1G>A	XP_016877014.1:n.3503-1G>A
XM_017021526.2:c.3503-1G>A	XP_016877015.1:n.3503-1G>A
XM_017021527.1:c.3488-1G>A	XP_016877016.1:n.3488-1G>A
XR_001750470.1:n.4780-1G>A
XR_001750471.2:n.4765-1G>A
XR_001750472.1:n.4817-1G>A