Canonical Allele Identifier: CA259634083

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45183827A>G , CM000676.2:g.45183827A>G	GRCh38
NC_000014.8:g.45653030A>G , CM000676.1:g.45653030A>G	GRCh37
NC_000014.7:g.44722780A>G	NCBI36
NG_007417.1:g.52895A>G , LRG_502:g.52895A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_020937.4:c.4440A>G MANE Select	NP_065988.1:p.Gln1480=
ENST00000267430.10:c.4440A>G MANE Select	ENSP00000267430.5:p.Gln1480=
NM_001308133.1:c.4362A>G	NP_001295062.1:p.Gln1454=
NM_001308133.2:c.4362A>G	NP_001295062.1:p.Gln1454=
NM_020937.2:c.4440A>G , LRG_502t1:c.4440A>G	NP_065988.1:p.Gln1480=
NM_020937.3:c.4440A>G	NP_065988.1:p.Gln1480=
ENST00000267430.9:c.4440A>G	ENSP00000267430.5:p.Gln1480=
ENST00000542564.6:c.4362A>G	ENSP00000442493.2:p.Gln1454=
ENST00000554809.5:c.1237A>G
ENST00000554809.6:c.2652A>G	ENSP00000450632.2:p.Gln884=
ENST00000555013.1:n.273A>G
ENST00000555484.2:c.218A>G
ENST00000556250.5:c.2988A>G	ENSP00000452033.1:p.Gln996=
ENST00000556250.6:c.4233A>G	ENSP00000452033.2:p.Gln1411=
ENST00000557110.2:c.218A>G
ENST00000696642.1:c.*3251A>G	ENSP00000512775.1:n.*3251A>G
ENST00000696644.1:n.176A>G
ENST00000696645.1:n.330A>G
ENST00000696647.1:c.4440A>G	ENSP00000512778.1:p.Gln1480=
ENST00000696648.1:c.*2465A>G	ENSP00000512779.1:n.*2465A>G
ENST00000696649.1:c.4284A>G	ENSP00000512780.1:p.Gln1428=
ENST00000696650.1:n.4388A>G
ENST00000696659.1:c.2438A>G
ENST00000696663.1:c.3371A>G
ENST00000696664.1:c.3272A>G
ENST00000696665.1:c.218A>G
ENST00000696675.1:c.*196A>G	ENSP00000512799.1:n.*196A>G
ENST00000696683.1:c.3257A>G
ENST00000696684.1:c.3257A>G
ENST00000696685.1:c.3257A>G
ENST00000696686.1:n.1177A>G
XM_011537034.1:c.4455A>G	XP_011535336.1:p.Gln1485=
XM_011537034.2:c.4455A>G	XP_011535336.1:p.Gln1485=
XM_011537035.1:c.4377A>G	XP_011535337.1:p.Gln1459=
XM_011537035.3:c.4377A>G	XP_011535337.1:p.Gln1459=
XM_011537036.1:c.4455A>G	XP_011535338.1:p.Gln1485=
XM_011537037.1:c.2469A>G	XP_011535339.1:p.Gln823=
XM_011537037.3:c.2469A>G	XP_011535339.1:p.Gln823=
XM_017021523.1:c.4455A>G	XP_016877012.1:p.Gln1485=
XM_017021524.2:c.3492A>G	XP_016877013.1:p.Gln1164=
XM_017021525.2:c.3270A>G	XP_016877014.1:p.Gln1090=
XM_017021526.2:c.3270A>G	XP_016877015.1:p.Gln1090=
XM_017021527.1:c.3255A>G	XP_016877016.1:p.Gln1085=
XR_001750470.1:n.4547A>G
XR_001750471.2:n.4532A>G
XR_001750472.1:n.4584A>G