Canonical Allele Identifier: CA7169043
Gene: FANCM HGNC NCBI

Linked Data

ClinVar Variation Id: 261381
dbSNP Id: rs112326758

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.45159093_45159094del , CM000676.2:g.45159093_45159094del GRCh38
NC_000014.8:g.45628296_45628297del , CM000676.1:g.45628296_45628297del GRCh37
NC_000014.7:g.44698046_44698047del NCBI36
NG_007417.1:g.28161_28162del , LRG_502:g.28161_28162del

Transcript Alleles

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