Canonical Allele Identifier: CA2400692315

Gene: NF2

Linked Data

• dbSNP Id: rs2067502905

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694843dup , CM000684.2:g.29694843dup	GRCh38
NC_000022.10:g.30090832dup , CM000684.1:g.30090832dup	GRCh37
NC_000022.9:g.28420832dup	NCBI36
NG_009057.1:g.96288dup , LRG_511:g.96288dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*41dup	ENSP00000354529.6:n.*41dup
ENST00000673312.2:c.*1323dup	ENSP00000500186.2:n.*1323dup
ENST00000338641.10:c.*41dup MANE Select	ENSP00000344666.5:n.*41dup
ENST00000361166.9:c.1247dup	ENSP00000354529.5:n.1247dup
ENST00000672461.1:c.*101dup	ENSP00000500919.1:n.*101dup
ENST00000672805.1:c.*1711dup	ENSP00000500295.1:n.*1711dup
ENST00000672896.1:c.*101dup	ENSP00000500117.1:n.*101dup
ENST00000673312.1:c.1848dup	ENSP00000500186.1:n.1848dup
ENST00000338641.8:c.*41dup	ENSP00000344666.4:n.*41dup
ENST00000361452.8:c.*101dup	ENSP00000354897.4:n.*101dup
ENST00000413209.6:c.*41dup	ENSP00000409921.2:n.*41dup
ENST00000432151.5:c.*185dup	ENSP00000395885.1:n.*185dup
NM_000268.3:c.*41dup , LRG_511t1:c.*41dup	NP_000259.1:n.*41dup
NM_016418.5:c.*101dup , LRG_511t2:c.*101dup	NP_057502.2:n.*101dup
NM_181828.2:c.*101dup	NP_861966.1:n.*101dup
NM_181829.2:c.*101dup	NP_861967.1:n.*101dup
NM_181830.2:c.*101dup	NP_861968.1:n.*101dup
NM_181832.2:c.*116dup	NP_861970.1:n.*116dup
NM_181833.2:c.*41dup	NP_861971.1:n.*41dup
NR_156186.1:n.2388dup
XM_017028809.2:c.*41dup	XP_016884298.1:n.*41dup
XM_017028810.1:c.*101dup	XP_016884299.1:n.*101dup
NM_000268.4:c.*41dup MANE Select	NP_000259.1:n.*41dup
NM_181828.3:c.*101dup	NP_861966.1:n.*101dup
NM_181829.3:c.*101dup	NP_861967.1:n.*101dup
NM_181830.3:c.*101dup	NP_861968.1:n.*101dup
NM_181832.3:c.*116dup	NP_861970.1:n.*116dup
NR_156186.2:n.2311dup
NM_181833.3:c.*41dup	NP_861971.1:n.*41dup