Canonical Allele Identifier: CA2801409374

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45166790_45166796dup , CM000676.2:g.45166790_45166796dup	GRCh38
NC_000014.8:g.45635993_45635999dup , CM000676.1:g.45635993_45635999dup	GRCh37
NC_000014.7:g.44705743_44705749dup	NCBI36
NG_007417.1:g.35858_35864dup , LRG_502:g.35858_35864dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1789-160_1789-154dup	ENSP00000450596.1:n.1789-160_1789-154dup
ENST00000556250.6:c.1582-160_1582-154dup	ENSP00000452033.2:n.1582-160_1582-154dup
ENST00000696641.1:c.1630-160_1630-154dup	ENSP00000512774.1:n.1630-160_1630-154dup
ENST00000696642.1:c.*600-160_*600-154dup	ENSP00000512775.1:n.*600-160_*600-154dup
ENST00000696646.1:c.*600-160_*600-154dup	ENSP00000512777.1:n.*600-160_*600-154dup
ENST00000696647.1:c.1789-160_1789-154dup	ENSP00000512778.1:n.1789-160_1789-154dup
ENST00000696648.1:c.1789-160_1789-154dup	ENSP00000512779.1:n.1789-160_1789-154dup
ENST00000696649.1:c.1789-160_1789-154dup	ENSP00000512780.1:n.1789-160_1789-154dup
ENST00000696650.1:n.1737-160_1737-154dup
ENST00000696658.1:n.2339-160_2339-154dup
ENST00000696662.1:c.1711-160_1711-154dup	ENSP00000512788.1:n.1711-160_1711-154dup
ENST00000696663.1:c.606-160_606-154dup
ENST00000696664.1:c.606-160_606-154dup
ENST00000696675.1:c.1789-160_1789-154dup	ENSP00000512799.1:n.1789-160_1789-154dup
ENST00000696683.1:c.606-160_606-154dup
ENST00000696684.1:c.606-160_606-154dup
ENST00000696685.1:c.606-160_606-154dup
ENST00000267430.10:c.1789-160_1789-154dup MANE Select	ENSP00000267430.5:n.1789-160_1789-154dup
ENST00000267430.9:c.1789-160_1789-154dup	ENSP00000267430.5:n.1789-160_1789-154dup
ENST00000542564.6:c.1711-160_1711-154dup	ENSP00000442493.2:n.1711-160_1711-154dup
ENST00000556036.5:c.1789-160_1789-154dup	ENSP00000450596.1:n.1789-160_1789-154dup
ENST00000556250.5:c.337-160_337-154dup	ENSP00000452033.1:n.337-160_337-154dup
NM_001308133.1:c.1711-160_1711-154dup	NP_001295062.1:n.1711-160_1711-154dup
NM_001308134.1:c.1789-160_1789-154dup	NP_001295063.1:n.1789-160_1789-154dup
NM_020937.2:c.1789-160_1789-154dup , LRG_502t1:c.1789-160_1789-154dup	NP_065988.1:n.1789-160_1789-154dup
NM_020937.3:c.1789-160_1789-154dup	NP_065988.1:n.1789-160_1789-154dup
XM_011537034.1:c.1789-160_1789-154dup	XP_011535336.1:n.1789-160_1789-154dup
XM_011537035.1:c.1711-160_1711-154dup	XP_011535337.1:n.1711-160_1711-154dup
XM_011537036.1:c.1789-160_1789-154dup	XP_011535338.1:n.1789-160_1789-154dup
XM_011537034.2:c.1789-160_1789-154dup	XP_011535336.1:n.1789-160_1789-154dup
XM_011537035.3:c.1711-160_1711-154dup	XP_011535337.1:n.1711-160_1711-154dup
XM_017021523.1:c.1789-160_1789-154dup	XP_016877012.1:n.1789-160_1789-154dup
XM_017021524.2:c.826-160_826-154dup	XP_016877013.1:n.826-160_826-154dup
XM_017021525.2:c.604-160_604-154dup	XP_016877014.1:n.604-160_604-154dup
XM_017021526.2:c.604-160_604-154dup	XP_016877015.1:n.604-160_604-154dup
XM_017021527.1:c.604-160_604-154dup	XP_016877016.1:n.604-160_604-154dup
XR_001750470.1:n.1881-160_1881-154dup
XR_001750471.2:n.1881-160_1881-154dup
XR_001750472.1:n.1881-160_1881-154dup
NM_020937.4:c.1789-160_1789-154dup MANE Select	NP_065988.1:n.1789-160_1789-154dup
NM_001308133.2:c.1711-160_1711-154dup	NP_001295062.1:n.1711-160_1711-154dup
NM_001308134.2:c.1789-160_1789-154dup	NP_001295063.1:n.1789-160_1789-154dup