Canonical Allele Identifier: CA2801409182

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159311_45159312insCCCAAACACACCCAACAC , CM000676.2:g.45159311_45159312insCCCAAACACACCCAACAC	GRCh38
NC_000014.8:g.45628514_45628515insCCCAAACACACCCAACAC , CM000676.1:g.45628514_45628515insCCCAAACACACCCAACAC	GRCh37
NC_000014.7:g.44698264_44698265insCCCAAACACACCCAACAC	NCBI36
NG_007417.1:g.28379_28380insCCCAAACACACCCAACAC , LRG_502:g.28379_28380insCCCAAACACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000450596.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000556250.6:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000452033.2:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696641.1:c.1422+31_1422+32insCCCAAACACACCCAACAC	ENSP00000512774.1:n.1422+31_1422+32insCCCAAACACACCCAACAC
ENST00000696642.1:c.*392+31_*392+32insCCCAAACACACCCAACAC	ENSP00000512775.1:n.*392+31_*392+32insCCCAAACACACCCAACAC
ENST00000696643.1:c.1612_1613insCCCAAACACACCCAACAC	ENSP00000512776.1:p.Asn538delinsThrGlnThrHisProThrHis
ENST00000696646.1:c.*392+31_*392+32insCCCAAACACACCCAACAC	ENSP00000512777.1:n.*392+31_*392+32insCCCAAACACACCCAACAC
ENST00000696647.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000512778.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696648.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000512779.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696649.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000512780.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696650.1:n.1529+31_1529+32insCCCAAACACACCCAACAC
ENST00000696658.1:n.2131+31_2131+32insCCCAAACACACCCAACAC
ENST00000696662.1:c.1503+31_1503+32insCCCAAACACACCCAACAC	ENSP00000512788.1:n.1503+31_1503+32insCCCAAACACACCCAACAC
ENST00000696663.1:c.398+31_398+32insCCCAAACACACCCAACAC
ENST00000696664.1:c.398+31_398+32insCCCAAACACACCCAACAC
ENST00000696675.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000512799.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696681.1:c.*423_*424insCCCAAACACACCCAACAC	ENSP00000512804.1:n.*423_*424insCCCAAACACACCCAACAC
ENST00000696682.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000512805.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000696683.1:c.398+31_398+32insCCCAAACACACCCAACAC
ENST00000696684.1:c.398+31_398+32insCCCAAACACACCCAACAC
ENST00000696685.1:c.398+31_398+32insCCCAAACACACCCAACAC
ENST00000267430.10:c.1581+31_1581+32insCCCAAACACACCCAACAC MANE Select	ENSP00000267430.5:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000267430.9:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000267430.5:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000542564.6:c.1503+31_1503+32insCCCAAACACACCCAACAC	ENSP00000442493.2:n.1503+31_1503+32insCCCAAACACACCCAACAC
ENST00000556036.5:c.1581+31_1581+32insCCCAAACACACCCAACAC	ENSP00000450596.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
ENST00000556250.5:c.336+31_336+32insCCCAAACACACCCAACAC	ENSP00000452033.1:n.336+31_336+32insCCCAAACACACCCAACAC
NM_001308133.1:c.1503+31_1503+32insCCCAAACACACCCAACAC	NP_001295062.1:n.1503+31_1503+32insCCCAAACACACCCAACAC
NM_001308134.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	NP_001295063.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
NM_020937.2:c.1581+31_1581+32insCCCAAACACACCCAACAC , LRG_502t1:c.1581+31_1581+32insCCCAAACACACCCAACAC	NP_065988.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
NM_020937.3:c.1581+31_1581+32insCCCAAACACACCCAACAC	NP_065988.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
XM_011537034.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	XP_011535336.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
XM_011537035.1:c.1503+31_1503+32insCCCAAACACACCCAACAC	XP_011535337.1:n.1503+31_1503+32insCCCAAACACACCCAACAC
XM_011537036.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	XP_011535338.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
XM_011537034.2:c.1581+31_1581+32insCCCAAACACACCCAACAC	XP_011535336.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
XM_011537035.3:c.1503+31_1503+32insCCCAAACACACCCAACAC	XP_011535337.1:n.1503+31_1503+32insCCCAAACACACCCAACAC
XM_017021523.1:c.1581+31_1581+32insCCCAAACACACCCAACAC	XP_016877012.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
XM_017021524.2:c.618+31_618+32insCCCAAACACACCCAACAC	XP_016877013.1:n.618+31_618+32insCCCAAACACACCCAACAC
XM_017021525.2:c.396+31_396+32insCCCAAACACACCCAACAC	XP_016877014.1:n.396+31_396+32insCCCAAACACACCCAACAC
XM_017021526.2:c.396+31_396+32insCCCAAACACACCCAACAC	XP_016877015.1:n.396+31_396+32insCCCAAACACACCCAACAC
XM_017021527.1:c.396+31_396+32insCCCAAACACACCCAACAC	XP_016877016.1:n.396+31_396+32insCCCAAACACACCCAACAC
XR_001750470.1:n.1673+31_1673+32insCCCAAACACACCCAACAC
XR_001750471.2:n.1673+31_1673+32insCCCAAACACACCCAACAC
XR_001750472.1:n.1673+31_1673+32insCCCAAACACACCCAACAC
NM_020937.4:c.1581+31_1581+32insCCCAAACACACCCAACAC MANE Select	NP_065988.1:n.1581+31_1581+32insCCCAAACACACCCAACAC
NM_001308133.2:c.1503+31_1503+32insCCCAAACACACCCAACAC	NP_001295062.1:n.1503+31_1503+32insCCCAAACACACCCAACAC
NM_001308134.2:c.1581+31_1581+32insCCCAAACACACCCAACAC	NP_001295063.1:n.1581+31_1581+32insCCCAAACACACCCAACAC