Canonical Allele Identifier: CA2577681019

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29639042_29639043insT , CM000684.2:g.29639042_29639043insT	GRCh38
NC_000022.10:g.30035031_30035032insT , CM000684.1:g.30035031_30035032insT	GRCh37
NC_000022.9:g.28365031_28365032insT	NCBI36
NG_009057.1:g.40487_40488insT , LRG_511:g.40487_40488insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.241-48_241-47insT	ENSP00000354529.6:n.241-48_241-47insT
ENST00000673312.2:c.241-48_241-47insT	ENSP00000500186.2:n.241-48_241-47insT
ENST00000338641.10:c.241-48_241-47insT MANE Select	ENSP00000344666.5:n.241-48_241-47insT
ENST00000672461.1:c.241-48_241-47insT	ENSP00000500919.1:n.241-48_241-47insT
ENST00000672805.1:c.*123-48_*123-47insT	ENSP00000500295.1:n.*123-48_*123-47insT
ENST00000672896.1:c.241-48_241-47insT	ENSP00000500117.1:n.241-48_241-47insT
ENST00000673312.1:c.154-48_154-47insT	ENSP00000500186.1:n.154-48_154-47insT
ENST00000334961.11:c.115-3160_115-3159insT	ENSP00000335652.7:n.115-3160_115-3159insT
ENST00000338641.8:c.241-48_241-47insT	ENSP00000344666.4:n.241-48_241-47insT
ENST00000353887.8:c.115-3160_115-3159insT	ENSP00000340626.4:n.115-3160_115-3159insT
ENST00000361166.8:c.241-48_241-47insT	ENSP00000354529.4:n.241-48_241-47insT
ENST00000361452.8:c.240+2166_240+2167insT	ENSP00000354897.4:n.240+2166_240+2167insT
ENST00000361676.8:c.115-48_115-47insT	ENSP00000355183.4:n.115-48_115-47insT
ENST00000397789.3:c.241-48_241-47insT	ENSP00000380891.3:n.241-48_241-47insT
ENST00000403435.5:c.241-48_241-47insT	ENSP00000384029.1:n.241-48_241-47insT
ENST00000403999.7:c.241-48_241-47insT	ENSP00000384797.3:n.241-48_241-47insT
ENST00000413209.6:c.241-48_241-47insT	ENSP00000409921.2:n.241-48_241-47insT
ENST00000432151.5:c.115-3160_115-3159insT	ENSP00000395885.1:n.115-3160_115-3159insT
NM_000268.3:c.241-48_241-47insT , LRG_511t1:c.241-48_241-47insT	NP_000259.1:n.241-48_241-47insT
NM_016418.5:c.241-48_241-47insT , LRG_511t2:c.241-48_241-47insT	NP_057502.2:n.241-48_241-47insT
NM_181825.2:c.241-48_241-47insT	NP_861546.1:n.241-48_241-47insT
NM_181828.2:c.115-48_115-47insT	NP_861966.1:n.115-48_115-47insT
NM_181829.2:c.240+2166_240+2167insT	NP_861967.1:n.240+2166_240+2167insT
NM_181830.2:c.115-3160_115-3159insT	NP_861968.1:n.115-3160_115-3159insT
NM_181831.2:c.115-3160_115-3159insT	NP_861969.1:n.115-3160_115-3159insT
NM_181832.2:c.241-48_241-47insT	NP_861970.1:n.241-48_241-47insT
NM_181833.2:c.241-48_241-47insT	NP_861971.1:n.241-48_241-47insT
NR_156186.1:n.800-48_800-47insT
XM_017028809.2:c.127-48_127-47insT	XP_016884298.1:n.127-48_127-47insT
XM_017028810.1:c.127-48_127-47insT	XP_016884299.1:n.127-48_127-47insT
NM_000268.4:c.241-48_241-47insT MANE Select	NP_000259.1:n.241-48_241-47insT
NM_181825.3:c.241-48_241-47insT	NP_861546.1:n.241-48_241-47insT
NM_181828.3:c.115-48_115-47insT	NP_861966.1:n.115-48_115-47insT
NM_181829.3:c.240+2166_240+2167insT	NP_861967.1:n.240+2166_240+2167insT
NM_181830.3:c.115-3160_115-3159insT	NP_861968.1:n.115-3160_115-3159insT
NM_181831.3:c.115-3160_115-3159insT	NP_861969.1:n.115-3160_115-3159insT
NM_181832.3:c.241-48_241-47insT	NP_861970.1:n.241-48_241-47insT
NR_156186.2:n.723-48_723-47insT
NM_181833.3:c.241-48_241-47insT	NP_861971.1:n.241-48_241-47insT