Canonical Allele Identifier: CA645601154
Gene: NF2 HGNC NCBI

Linked Data

COSMIC: COSM22219

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.29674831_29674846del , CM000684.2:g.29674831_29674846del GRCh38
NC_000022.10:g.30070820_30070835del , CM000684.1:g.30070820_30070835del GRCh37
NC_000022.9:g.28400820_28400835del NCBI36
NG_009057.1:g.76276_76291del , LRG_511:g.76276_76291del

Transcript Alleles

HGVS Amino-acid change
ENST00000361166.10:c.1206-5_1216del
ENST00000673312.2:c.*835-5_*845del
ENST00000338641.10:c.1341-5_1351del
ENST00000361166.9:c.759-5_769del
ENST00000672461.1:c.1341-5_1351del
ENST00000672805.1:c.*1223-5_*1233del
ENST00000672896.1:c.1341-5_1351del
ENST00000673312.1:c.1360-5_1370del
ENST00000334961.11:c.1092-5_1102del
ENST00000338641.8:c.1341-5_1351del
ENST00000353887.8:c.1092-5_1102del
ENST00000361166.8:c.1341-5_1351del
ENST00000361452.8:c.1218-5_1228del
ENST00000361676.8:c.1215-5_1225del
ENST00000397789.3:c.1341-5_1351del
ENST00000403435.5:c.1254-5_1264del
ENST00000403999.7:c.1341-5_1351del
ENST00000413209.6:c.448-19921_448-19906del ENSP00000409921.2:n.448-19921_448-19906del
ENST00000432151.5:c.523-5_533del
NM_000268.3:c.1341-5_1351del , LRG_511t1:c.1341-5_1351del
NM_016418.5:c.1341-5_1351del , LRG_511t2:c.1341-5_1351del
NM_181825.2:c.1341-5_1351del
NM_181828.2:c.1215-5_1225del
NM_181829.2:c.1218-5_1228del
NM_181830.2:c.1092-5_1102del
NM_181831.2:c.1092-5_1102del
NM_181832.2:c.1341-5_1351del
NM_181833.2:c.448-19921_448-19906del NP_861971.1:n.448-19921_448-19906del
NR_156186.1:n.1900-5_1910del
XM_017028809.2:c.1227-5_1237del
XM_017028810.1:c.1227-5_1237del
NM_000268.4:c.1341-5_1351del
NM_181825.3:c.1341-5_1351del
NM_181828.3:c.1215-5_1225del
NM_181829.3:c.1218-5_1228del
NM_181830.3:c.1092-5_1102del
NM_181831.3:c.1092-5_1102del
NM_181832.3:c.1341-5_1351del
NR_156186.2:n.1823-5_1833del
NM_181833.3:c.448-19921_448-19906del NP_861971.1:n.448-19921_448-19906del