Canonical Allele Identifier: CA2400692319

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694847G= , CM000684.2:g.29694847G=	GRCh38
NC_000022.10:g.30090836G= , CM000684.1:g.30090836G=	GRCh37
NC_000022.9:g.28420836G=	NCBI36
NG_009057.1:g.96292G= , LRG_511:g.96292G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*45G=	ENSP00000354529.6:n.*45G=
ENST00000673312.2:c.*1327G=	ENSP00000500186.2:n.*1327G=
ENST00000338641.10:c.*45G= MANE Select	ENSP00000344666.5:n.*45G=
ENST00000361166.9:c.1251G=	ENSP00000354529.5:n.1251G=
ENST00000672461.1:c.*105G=	ENSP00000500919.1:n.*105G=
ENST00000672805.1:c.*1715G=	ENSP00000500295.1:n.*1715G=
ENST00000672896.1:c.*105G=	ENSP00000500117.1:n.*105G=
ENST00000673312.1:c.1852G=	ENSP00000500186.1:n.1852G=
ENST00000338641.8:c.*45G=	ENSP00000344666.4:n.*45G=
ENST00000361452.8:c.*105G=	ENSP00000354897.4:n.*105G=
ENST00000413209.6:c.*45G=	ENSP00000409921.2:n.*45G=
ENST00000432151.5:c.*189G=	ENSP00000395885.1:n.*189G=
NM_000268.3:c.*45G= , LRG_511t1:c.*45G=	NP_000259.1:n.*45G=
NM_016418.5:c.*105G= , LRG_511t2:c.*105G=	NP_057502.2:n.*105G=
NM_181828.2:c.*105G=	NP_861966.1:n.*105G=
NM_181829.2:c.*105G=	NP_861967.1:n.*105G=
NM_181830.2:c.*105G=	NP_861968.1:n.*105G=
NM_181832.2:c.*120G=	NP_861970.1:n.*120G=
NM_181833.2:c.*45G=	NP_861971.1:n.*45G=
NR_156186.1:n.2392G=
XM_017028809.2:c.*45G=	XP_016884298.1:n.*45G=
XM_017028810.1:c.*105G=	XP_016884299.1:n.*105G=
NM_000268.4:c.*45G= MANE Select	NP_000259.1:n.*45G=
NM_181828.3:c.*105G=	NP_861966.1:n.*105G=
NM_181829.3:c.*105G=	NP_861967.1:n.*105G=
NM_181830.3:c.*105G=	NP_861968.1:n.*105G=
NM_181832.3:c.*120G=	NP_861970.1:n.*120G=
NR_156186.2:n.2315G=
NM_181833.3:c.*45G=	NP_861971.1:n.*45G=