Canonical Allele Identifier: CA2695230620

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29639127_29639130del , CM000684.2:g.29639127_29639130del	GRCh38
NC_000022.10:g.30035116_30035119del , CM000684.1:g.30035116_30035119del	GRCh37
NC_000022.9:g.28365116_28365119del	NCBI36
NG_009057.1:g.40572_40575del , LRG_511:g.40572_40575del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361166.10:c.278_281del	ENSP00000354529.6:p.Thr93IlefsTer29
ENST00000673312.2:c.278_281del	ENSP00000500186.2:p.Thr93IlefsTer29
ENST00000338641.10:c.278_281del MANE Select	ENSP00000344666.5:p.Thr93IlefsTer29
ENST00000672461.1:c.278_281del	ENSP00000500919.1:p.Thr93IlefsTer29
ENST00000672805.1:c.*160_*163del	ENSP00000500295.1:n.*160_*163del
ENST00000672896.1:c.278_281del	ENSP00000500117.1:p.Thr93IlefsTer29
ENST00000673312.1:c.191_194del	ENSP00000500186.1:p.Thr64IlefsTer29
ENST00000334961.11:c.115-3075_115-3072del	ENSP00000335652.7:n.115-3075_115-3072del
ENST00000338641.8:c.278_281del	ENSP00000344666.4:p.Thr93IlefsTer29
ENST00000353887.8:c.115-3075_115-3072del	ENSP00000340626.4:n.115-3075_115-3072del
ENST00000361166.8:c.278_281del	ENSP00000354529.4:p.Thr93IlefsTer29
ENST00000361452.8:c.240+2251_240+2254del	ENSP00000354897.4:n.240+2251_240+2254del
ENST00000361676.8:c.152_155del	ENSP00000355183.4:p.Thr51IlefsTer29
ENST00000397789.3:c.278_281del	ENSP00000380891.3:p.Thr93IlefsTer29
ENST00000403435.5:c.278_281del	ENSP00000384029.1:p.Thr93IlefsTer29
ENST00000403999.7:c.278_281del	ENSP00000384797.3:p.Thr93IlefsTer29
ENST00000413209.6:c.278_281del	ENSP00000409921.2:p.Thr93IlefsTer29
ENST00000432151.5:c.115-3075_115-3072del	ENSP00000395885.1:n.115-3075_115-3072del
NM_000268.3:c.278_281del , LRG_511t1:c.278_281del	NP_000259.1:p.Thr93IlefsTer29
NM_016418.5:c.278_281del , LRG_511t2:c.278_281del	NP_057502.2:p.Thr93IlefsTer29
NM_181825.2:c.278_281del	NP_861546.1:p.Thr93IlefsTer29
NM_181828.2:c.152_155del	NP_861966.1:p.Thr51IlefsTer29
NM_181829.2:c.240+2251_240+2254del	NP_861967.1:n.240+2251_240+2254del
NM_181830.2:c.115-3075_115-3072del	NP_861968.1:n.115-3075_115-3072del
NM_181831.2:c.115-3075_115-3072del	NP_861969.1:n.115-3075_115-3072del
NM_181832.2:c.278_281del	NP_861970.1:p.Thr93IlefsTer29
NM_181833.2:c.278_281del	NP_861971.1:p.Thr93IlefsTer29
NR_156186.1:n.837_840del
XM_017028809.2:c.164_167del	XP_016884298.1:p.Thr55IlefsTer29
XM_017028810.1:c.164_167del	XP_016884299.1:p.Thr55IlefsTer29
NM_000268.4:c.278_281del MANE Select	NP_000259.1:p.Thr93IlefsTer29
NM_181825.3:c.278_281del	NP_861546.1:p.Thr93IlefsTer29
NM_181828.3:c.152_155del	NP_861966.1:p.Thr51IlefsTer29
NM_181829.3:c.240+2251_240+2254del	NP_861967.1:n.240+2251_240+2254del
NM_181830.3:c.115-3075_115-3072del	NP_861968.1:n.115-3075_115-3072del
NM_181831.3:c.115-3075_115-3072del	NP_861969.1:n.115-3075_115-3072del
NM_181832.3:c.278_281del	NP_861970.1:p.Thr93IlefsTer29
NR_156186.2:n.760_763del
NM_181833.3:c.278_281del	NP_861971.1:p.Thr93IlefsTer29