Canonical Allele Identifier: CA645601155

Gene: NF2

Linked Data

• COSMIC: COSM49114

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29674837_29674942del , CM000684.2:g.29674837_29674942del	GRCh38
NC_000022.10:g.30070826_30070931del , CM000684.1:g.30070826_30070931del	GRCh37
NC_000022.9:g.28400826_28400931del	NCBI36
NG_009057.1:g.76282_76387del , LRG_511:g.76282_76387del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1207_1311+1del
ENST00000673312.2:c.*836_*940+1del
ENST00000338641.10:c.1342_1446+1del
ENST00000361166.9:c.760_864+1del
ENST00000672461.1:c.1342_1446+1del
ENST00000672805.1:c.*1224_*1328+1del
ENST00000672896.1:c.1342_1446+1del
ENST00000673312.1:c.1361_1465+1del
ENST00000334961.11:c.1093_1197+1del
ENST00000338641.8:c.1342_1446+1del
ENST00000353887.8:c.1093_1197+1del
ENST00000361166.8:c.1342_1446+1del
ENST00000361452.8:c.1219_1323+1del
ENST00000361676.8:c.1216_1320+1del
ENST00000397789.3:c.1342_1446+1del
ENST00000403435.5:c.1255_1359+1del
ENST00000403999.7:c.1342_1446+1del
ENST00000413209.6:c.448-19915_448-19810del	ENSP00000409921.2:n.448-19915_448-19810de...
ENST00000432151.5:c.524_628+1del
NM_000268.3:c.1342_1446+1del , LRG_511t1:c.1342_1446+1del
NM_016418.5:c.1342_1446+1del , LRG_511t2:c.1342_1446+1del
NM_181825.2:c.1342_1446+1del
NM_181828.2:c.1216_1320+1del
NM_181829.2:c.1219_1323+1del
NM_181830.2:c.1093_1197+1del
NM_181831.2:c.1093_1197+1del
NM_181832.2:c.1342_1446+1del
NM_181833.2:c.448-19915_448-19810del	NP_861971.1:n.448-19915_448-19810del
NR_156186.1:n.1901_2005+1del
XM_017028809.2:c.1228_1332+1del
XM_017028810.1:c.1228_1332+1del
NM_000268.4:c.1342_1446+1del
NM_181825.3:c.1342_1446+1del
NM_181828.3:c.1216_1320+1del
NM_181829.3:c.1219_1323+1del
NM_181830.3:c.1093_1197+1del
NM_181831.3:c.1093_1197+1del
NM_181832.3:c.1342_1446+1del
NR_156186.2:n.1824_1928+1del
NM_181833.3:c.448-19915_448-19810del	NP_861971.1:n.448-19915_448-19810del