Canonical Allele Identifier: CA2133607388

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159283_45159286delinsAATT , CM000676.2:g.45159283_45159286delinsAATT	GRCh38
NC_000014.8:g.45628486_45628489delinsAATT , CM000676.1:g.45628486_45628489delinsAATT	GRCh37
NC_000014.7:g.44698236_44698239delinsAATT	NCBI36
NG_007417.1:g.28351_28354delinsAATT , LRG_502:g.28351_28354delinsAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1581+3_1581+6delinsAATT	ENSP00000450596.1:n.1581+3_1581+6delinsAATT
ENST00000556250.6:c.1581+3_1581+6delinsAATT	ENSP00000452033.2:n.1581+3_1581+6delinsAATT
ENST00000696641.1:c.1422+3_1422+6delinsAATT	ENSP00000512774.1:n.1422+3_1422+6delinsAATT
ENST00000696642.1:c.*392+3_*392+6delinsAATT	ENSP00000512775.1:n.*392+3_*392+6delinsAATT
ENST00000696643.1:c.1584_1587delinsAATT	ENSP00000512776.1:p.Val528=
ENST00000696646.1:c.*392+3_*392+6delinsAATT	ENSP00000512777.1:n.*392+3_*392+6delinsAATT
ENST00000696647.1:c.1581+3_1581+6delinsAATT	ENSP00000512778.1:n.1581+3_1581+6delinsAATT
ENST00000696648.1:c.1581+3_1581+6delinsAATT	ENSP00000512779.1:n.1581+3_1581+6delinsAATT
ENST00000696649.1:c.1581+3_1581+6delinsAATT	ENSP00000512780.1:n.1581+3_1581+6delinsAATT
ENST00000696650.1:n.1529+3_1529+6delinsAATT
ENST00000696658.1:n.2131+3_2131+6delinsAATT
ENST00000696662.1:c.1503+3_1503+6delinsAATT	ENSP00000512788.1:n.1503+3_1503+6delinsAATT
ENST00000696663.1:c.398+3_398+6delinsAATT
ENST00000696664.1:c.398+3_398+6delinsAATT
ENST00000696675.1:c.1581+3_1581+6delinsAATT	ENSP00000512799.1:n.1581+3_1581+6delinsAATT
ENST00000696681.1:c.*395_*398delinsAATT	ENSP00000512804.1:n.*395_*398delinsAATT
ENST00000696682.1:c.1581+3_1581+6delinsAATT	ENSP00000512805.1:n.1581+3_1581+6delinsAATT
ENST00000696683.1:c.398+3_398+6delinsAATT
ENST00000696684.1:c.398+3_398+6delinsAATT
ENST00000696685.1:c.398+3_398+6delinsAATT
ENST00000267430.10:c.1581+3_1581+6delinsAATT MANE Select	ENSP00000267430.5:n.1581+3_1581+6delinsAATT
ENST00000267430.9:c.1581+3_1581+6delinsAATT	ENSP00000267430.5:n.1581+3_1581+6delinsAATT
ENST00000542564.6:c.1503+3_1503+6delinsAATT	ENSP00000442493.2:n.1503+3_1503+6delinsAATT
ENST00000556036.5:c.1581+3_1581+6delinsAATT	ENSP00000450596.1:n.1581+3_1581+6delinsAATT
ENST00000556250.5:c.336+3_336+6delinsAATT	ENSP00000452033.1:n.336+3_336+6delinsAATT
NM_001308133.1:c.1503+3_1503+6delinsAATT	NP_001295062.1:n.1503+3_1503+6delinsAATT
NM_001308134.1:c.1581+3_1581+6delinsAATT	NP_001295063.1:n.1581+3_1581+6delinsAATT
NM_020937.2:c.1581+3_1581+6delinsAATT , LRG_502t1:c.1581+3_1581+6delinsAATT	NP_065988.1:n.1581+3_1581+6delinsAATT
NM_020937.3:c.1581+3_1581+6delinsAATT	NP_065988.1:n.1581+3_1581+6delinsAATT
XM_011537034.1:c.1581+3_1581+6delinsAATT	XP_011535336.1:n.1581+3_1581+6delinsAATT
XM_011537035.1:c.1503+3_1503+6delinsAATT	XP_011535337.1:n.1503+3_1503+6delinsAATT
XM_011537036.1:c.1581+3_1581+6delinsAATT	XP_011535338.1:n.1581+3_1581+6delinsAATT
XM_011537034.2:c.1581+3_1581+6delinsAATT	XP_011535336.1:n.1581+3_1581+6delinsAATT
XM_011537035.3:c.1503+3_1503+6delinsAATT	XP_011535337.1:n.1503+3_1503+6delinsAATT
XM_017021523.1:c.1581+3_1581+6delinsAATT	XP_016877012.1:n.1581+3_1581+6delinsAATT
XM_017021524.2:c.618+3_618+6delinsAATT	XP_016877013.1:n.618+3_618+6delinsAATT
XM_017021525.2:c.396+3_396+6delinsAATT	XP_016877014.1:n.396+3_396+6delinsAATT
XM_017021526.2:c.396+3_396+6delinsAATT	XP_016877015.1:n.396+3_396+6delinsAATT
XM_017021527.1:c.396+3_396+6delinsAATT	XP_016877016.1:n.396+3_396+6delinsAATT
XR_001750470.1:n.1673+3_1673+6delinsAATT
XR_001750471.2:n.1673+3_1673+6delinsAATT
XR_001750472.1:n.1673+3_1673+6delinsAATT
NM_020937.4:c.1581+3_1581+6delinsAATT MANE Select	NP_065988.1:n.1581+3_1581+6delinsAATT
NM_001308133.2:c.1503+3_1503+6delinsAATT	NP_001295062.1:n.1503+3_1503+6delinsAATT
NM_001308134.2:c.1581+3_1581+6delinsAATT	NP_001295063.1:n.1581+3_1581+6delinsAATT