Canonical Allele Identifier: CA658166171

Gene: NF2

Linked Data

• COSMIC: COSN23130481

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29697233_29697234insT , CM000684.2:g.29697233_29697234insT	GRCh38
NC_000022.10:g.30093222_30093223insT , CM000684.1:g.30093222_30093223insT	GRCh37
NC_000022.9:g.28423222_28423223insT	NCBI36
NG_009057.1:g.98678_98679insT , LRG_511:g.98678_98679insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338641.10:c.*2431_*2432insT MANE Select	ENSP00000344666.5:n.*2431_*2432insT
ENST00000672461.1:c.*502-28_*502-27insT	ENSP00000500919.1:n.*502-28_*502-27insT
ENST00000672896.1:c.*2491_*2492insT	ENSP00000500117.1:n.*2491_*2492insT
ENST00000338641.8:c.*2431_*2432insT	ENSP00000344666.4:n.*2431_*2432insT
ENST00000361452.8:c.*2491_*2492insT	ENSP00000354897.4:n.*2491_*2492insT
ENST00000413209.6:c.*2431_*2432insT	ENSP00000409921.2:n.*2431_*2432insT
NM_000268.3:c.*2431_*2432insT , LRG_511t1:c.*2431_*2432insT	NP_000259.1:n.*2431_*2432insT
NM_016418.5:c.*2491_*2492insT , LRG_511t2:c.*2491_*2492insT	NP_057502.2:n.*2491_*2492insT
NM_181828.2:c.*2491_*2492insT	NP_861966.1:n.*2491_*2492insT
NM_181829.2:c.*2491_*2492insT	NP_861967.1:n.*2491_*2492insT
NM_181830.2:c.*2491_*2492insT	NP_861968.1:n.*2491_*2492insT
NM_181832.2:c.*2506_*2507insT	NP_861970.1:n.*2506_*2507insT
NM_181833.2:c.*2431_*2432insT	NP_861971.1:n.*2431_*2432insT
NR_156186.1:n.4778_4779insT
XM_017028810.1:c.*2491_*2492insT	XP_016884299.1:n.*2491_*2492insT
NM_000268.4:c.*2431_*2432insT MANE Select	NP_000259.1:n.*2431_*2432insT
NM_181828.3:c.*2491_*2492insT	NP_861966.1:n.*2491_*2492insT
NM_181829.3:c.*2491_*2492insT	NP_861967.1:n.*2491_*2492insT
NM_181830.3:c.*2491_*2492insT	NP_861968.1:n.*2491_*2492insT
NM_181832.3:c.*2506_*2507insT	NP_861970.1:n.*2506_*2507insT
NR_156186.2:n.4701_4702insT
NM_181833.3:c.*2431_*2432insT	NP_861971.1:n.*2431_*2432insT