Canonical Allele Identifier: CA2133606974

Gene: FANCM

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45159014_45159015delinsCT , CM000676.2:g.45159014_45159015delinsCT	GRCh38
NC_000014.8:g.45628217_45628218delinsCT , CM000676.1:g.45628217_45628218delinsCT	GRCh37
NC_000014.7:g.44697967_44697968delinsCT	NCBI36
NG_007417.1:g.28082_28083delinsCT , LRG_502:g.28082_28083delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556036.6:c.1397-82_1397-81delinsCT	ENSP00000450596.1:n.1397-82_1397-81delinsCT
ENST00000556250.6:c.1397-82_1397-81delinsCT	ENSP00000452033.2:n.1397-82_1397-81delinsCT
ENST00000696641.1:c.1238-82_1238-81delinsCT	ENSP00000512774.1:n.1238-82_1238-81delinsCT
ENST00000696642.1:c.*208-82_*208-81delinsCT	ENSP00000512775.1:n.*208-82_*208-81delinsCT
ENST00000696643.1:c.1397-82_1397-81delinsCT	ENSP00000512776.1:n.1397-82_1397-81delinsCT
ENST00000696646.1:c.*208-82_*208-81delinsCT	ENSP00000512777.1:n.*208-82_*208-81delinsCT
ENST00000696647.1:c.1397-82_1397-81delinsCT	ENSP00000512778.1:n.1397-82_1397-81delinsCT
ENST00000696648.1:c.1397-82_1397-81delinsCT	ENSP00000512779.1:n.1397-82_1397-81delinsCT
ENST00000696649.1:c.1397-82_1397-81delinsCT	ENSP00000512780.1:n.1397-82_1397-81delinsCT
ENST00000696650.1:n.1345-82_1345-81delinsCT
ENST00000696658.1:n.1947-82_1947-81delinsCT
ENST00000696662.1:c.1319-82_1319-81delinsCT	ENSP00000512788.1:n.1319-82_1319-81delinsCT
ENST00000696663.1:c.214-82_214-81delinsCT
ENST00000696664.1:c.214-82_214-81delinsCT
ENST00000696675.1:c.1397-82_1397-81delinsCT	ENSP00000512799.1:n.1397-82_1397-81delinsCT
ENST00000696680.1:c.1265-82_1265-81delinsCT	ENSP00000512803.1:n.1265-82_1265-81delinsCT
ENST00000696681.1:c.*208-82_*208-81delinsCT	ENSP00000512804.1:n.*208-82_*208-81delinsCT
ENST00000696682.1:c.1397-82_1397-81delinsCT	ENSP00000512805.1:n.1397-82_1397-81delinsCT
ENST00000696683.1:c.214-82_214-81delinsCT
ENST00000696684.1:c.214-82_214-81delinsCT
ENST00000696685.1:c.214-82_214-81delinsCT
ENST00000267430.10:c.1397-82_1397-81delinsCT MANE Select	ENSP00000267430.5:n.1397-82_1397-81delinsCT
ENST00000267430.9:c.1397-82_1397-81delinsCT	ENSP00000267430.5:n.1397-82_1397-81delinsCT
ENST00000542564.6:c.1319-82_1319-81delinsCT	ENSP00000442493.2:n.1319-82_1319-81delinsCT
ENST00000556036.5:c.1397-82_1397-81delinsCT	ENSP00000450596.1:n.1397-82_1397-81delinsCT
ENST00000556250.5:c.152-82_152-81delinsCT	ENSP00000452033.1:n.152-82_152-81delinsCT
NM_001308133.1:c.1319-82_1319-81delinsCT	NP_001295062.1:n.1319-82_1319-81delinsCT
NM_001308134.1:c.1397-82_1397-81delinsCT	NP_001295063.1:n.1397-82_1397-81delinsCT
NM_020937.2:c.1397-82_1397-81delinsCT , LRG_502t1:c.1397-82_1397-81delinsCT	NP_065988.1:n.1397-82_1397-81delinsCT
NM_020937.3:c.1397-82_1397-81delinsCT	NP_065988.1:n.1397-82_1397-81delinsCT
XM_011537034.1:c.1397-82_1397-81delinsCT	XP_011535336.1:n.1397-82_1397-81delinsCT
XM_011537035.1:c.1319-82_1319-81delinsCT	XP_011535337.1:n.1319-82_1319-81delinsCT
XM_011537036.1:c.1397-82_1397-81delinsCT	XP_011535338.1:n.1397-82_1397-81delinsCT
XM_011537034.2:c.1397-82_1397-81delinsCT	XP_011535336.1:n.1397-82_1397-81delinsCT
XM_011537035.3:c.1319-82_1319-81delinsCT	XP_011535337.1:n.1319-82_1319-81delinsCT
XM_017021523.1:c.1397-82_1397-81delinsCT	XP_016877012.1:n.1397-82_1397-81delinsCT
XM_017021524.2:c.434-82_434-81delinsCT	XP_016877013.1:n.434-82_434-81delinsCT
XM_017021525.2:c.212-82_212-81delinsCT	XP_016877014.1:n.212-82_212-81delinsCT
XM_017021526.2:c.212-82_212-81delinsCT	XP_016877015.1:n.212-82_212-81delinsCT
XM_017021527.1:c.212-82_212-81delinsCT	XP_016877016.1:n.212-82_212-81delinsCT
XR_001750470.1:n.1489-82_1489-81delinsCT
XR_001750471.2:n.1489-82_1489-81delinsCT
XR_001750472.1:n.1489-82_1489-81delinsCT
NM_020937.4:c.1397-82_1397-81delinsCT MANE Select	NP_065988.1:n.1397-82_1397-81delinsCT
NM_001308133.2:c.1319-82_1319-81delinsCT	NP_001295062.1:n.1319-82_1319-81delinsCT
NM_001308134.2:c.1397-82_1397-81delinsCT	NP_001295063.1:n.1397-82_1397-81delinsCT