Canonical Allele Identifier: CA1139770873

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29668333_29674941del , CM000684.2:g.29668333_29674941del	GRCh38
NC_000022.10:g.30064322_30070930del , CM000684.1:g.30064322_30070930del	GRCh37
NC_000022.9:g.28394322_28400930del	NCBI36
NG_009057.1:g.69778_76386del , LRG_511:g.69778_76386del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.751_1311del
ENST00000673312.2:c.*380_*940del
ENST00000338641.10:c.886_1446del
ENST00000361166.9:c.304_864del
ENST00000672461.1:c.886_1446del
ENST00000672805.1:c.*768_*1328del
ENST00000672896.1:c.886_1446del
ENST00000673312.1:c.905_1465del
ENST00000334961.11:c.637_1197del
ENST00000338641.8:c.886_1446del
ENST00000353887.8:c.637_1197del
ENST00000361166.8:c.886_1446del
ENST00000361452.8:c.763_1323del
ENST00000361676.8:c.760_1320del
ENST00000397789.3:c.886_1446del
ENST00000403435.5:c.886_1359del
ENST00000403999.7:c.886_1446del
ENST00000413209.6:c.447+26048_448-19811del	ENSP00000409921.2:n.447+26048_448-19811de...
ENST00000432151.5:c.409_628del
NM_000268.3:c.886_1446del , LRG_511t1:c.886_1446del
NM_016418.5:c.886_1446del , LRG_511t2:c.886_1446del
NM_181825.2:c.886_1446del
NM_181828.2:c.760_1320del
NM_181829.2:c.763_1323del
NM_181830.2:c.637_1197del
NM_181831.2:c.637_1197del
NM_181832.2:c.886_1446del
NM_181833.2:c.447+26048_448-19811del	NP_861971.1:n.447+26048_448-19811del
NR_156186.1:n.1445_2005del
XM_017028809.2:c.772_1332del
XM_017028810.1:c.772_1332del
NM_000268.4:c.886_1446del
NM_181825.3:c.886_1446del
NM_181828.3:c.760_1320del
NM_181829.3:c.763_1323del
NM_181830.3:c.637_1197del
NM_181831.3:c.637_1197del
NM_181832.3:c.886_1446del
NR_156186.2:n.1368_1928del
NM_181833.3:c.447+26048_448-19811del	NP_861971.1:n.447+26048_448-19811del