Canonical Allele Identifier: CA514187653

Gene: NF2

Linked Data

• COSMIC: COSM22308
• MyVariant Identifiers: chr22:g.30070826del (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.1207del
ENST00000673312.2:c.*836del
ENST00000338641.10:c.1342del
ENST00000361166.9:c.760del
ENST00000672461.1:c.1342del
ENST00000672805.1:c.*1224del
ENST00000672896.1:c.1342del
ENST00000673312.1:c.1361del
ENST00000334961.11:c.1093del
ENST00000338641.8:c.1342del
ENST00000353887.8:c.1093del
ENST00000361166.8:c.1342del
ENST00000361452.8:c.1219del
ENST00000361676.8:c.1216del
ENST00000397789.3:c.1342del
ENST00000403435.5:c.1255del
ENST00000403999.7:c.1342del
ENST00000413209.6:c.448-19915del	ENSP00000409921.2:n.448-19915del
ENST00000432151.5:c.524del
NM_000268.3:c.1342del , LRG_511t1:c.1342del
NM_016418.5:c.1342del , LRG_511t2:c.1342del
NM_181825.2:c.1342del
NM_181828.2:c.1216del
NM_181829.2:c.1219del
NM_181830.2:c.1093del
NM_181831.2:c.1093del
NM_181832.2:c.1342del
NM_181833.2:c.448-19915del	NP_861971.1:n.448-19915del
NR_156186.1:n.1901del
XM_017028809.2:c.1228del
XM_017028810.1:c.1228del
NM_000268.4:c.1342del
NM_181825.3:c.1342del
NM_181828.3:c.1216del
NM_181829.3:c.1219del
NM_181830.3:c.1093del
NM_181831.3:c.1093del
NM_181832.3:c.1342del
NR_156186.2:n.1824del
NM_181833.3:c.448-19915del	NP_861971.1:n.448-19915del