Canonical Allele Identifier: CA2818694854

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694903dup , CM000684.2:g.29694903dup	GRCh38
NC_000022.10:g.30090892dup , CM000684.1:g.30090892dup	GRCh37
NC_000022.9:g.28420892dup	NCBI36
NG_009057.1:g.96348dup , LRG_511:g.96348dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*101dup	ENSP00000354529.6:n.*101dup
ENST00000673312.2:c.*1383dup	ENSP00000500186.2:n.*1383dup
ENST00000338641.10:c.*101dup MANE Select	ENSP00000344666.5:n.*101dup
ENST00000361166.9:c.1307dup	ENSP00000354529.5:n.1307dup
ENST00000672461.1:c.*161dup	ENSP00000500919.1:n.*161dup
ENST00000672805.1:c.*1771dup	ENSP00000500295.1:n.*1771dup
ENST00000672896.1:c.*161dup	ENSP00000500117.1:n.*161dup
ENST00000673312.1:c.1908dup	ENSP00000500186.1:n.1908dup
ENST00000338641.8:c.*101dup	ENSP00000344666.4:n.*101dup
ENST00000361452.8:c.*161dup	ENSP00000354897.4:n.*161dup
ENST00000413209.6:c.*101dup	ENSP00000409921.2:n.*101dup
ENST00000432151.5:c.*245dup	ENSP00000395885.1:n.*245dup
NM_000268.3:c.*101dup , LRG_511t1:c.*101dup	NP_000259.1:n.*101dup
NM_016418.5:c.*161dup , LRG_511t2:c.*161dup	NP_057502.2:n.*161dup
NM_181828.2:c.*161dup	NP_861966.1:n.*161dup
NM_181829.2:c.*161dup	NP_861967.1:n.*161dup
NM_181830.2:c.*161dup	NP_861968.1:n.*161dup
NM_181832.2:c.*176dup	NP_861970.1:n.*176dup
NM_181833.2:c.*101dup	NP_861971.1:n.*101dup
NR_156186.1:n.2448dup
XM_017028809.2:c.*101dup	XP_016884298.1:n.*101dup
XM_017028810.1:c.*161dup	XP_016884299.1:n.*161dup
NM_000268.4:c.*101dup MANE Select	NP_000259.1:n.*101dup
NM_181828.3:c.*161dup	NP_861966.1:n.*161dup
NM_181829.3:c.*161dup	NP_861967.1:n.*161dup
NM_181830.3:c.*161dup	NP_861968.1:n.*161dup
NM_181832.3:c.*176dup	NP_861970.1:n.*176dup
NR_156186.2:n.2371dup
NM_181833.3:c.*101dup	NP_861971.1:n.*101dup