Canonical Allele Identifier: CA2400692357

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694923A= , CM000684.2:g.29694923A=	GRCh38
NC_000022.10:g.30090912A= , CM000684.1:g.30090912A=	GRCh37
NC_000022.9:g.28420912A=	NCBI36
NG_009057.1:g.96368A= , LRG_511:g.96368A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*121A=	ENSP00000354529.6:n.*121A=
ENST00000673312.2:c.*1403A=	ENSP00000500186.2:n.*1403A=
ENST00000338641.10:c.*121A= MANE Select	ENSP00000344666.5:n.*121A=
ENST00000361166.9:c.1327A=	ENSP00000354529.5:n.1327A=
ENST00000672461.1:c.*181A=	ENSP00000500919.1:n.*181A=
ENST00000672805.1:c.*1791A=	ENSP00000500295.1:n.*1791A=
ENST00000672896.1:c.*181A=	ENSP00000500117.1:n.*181A=
ENST00000673312.1:c.1928A=	ENSP00000500186.1:n.1928A=
ENST00000338641.8:c.*121A=	ENSP00000344666.4:n.*121A=
ENST00000361452.8:c.*181A=	ENSP00000354897.4:n.*181A=
ENST00000413209.6:c.*121A=	ENSP00000409921.2:n.*121A=
ENST00000432151.5:c.*265A=	ENSP00000395885.1:n.*265A=
NM_000268.3:c.*121A= , LRG_511t1:c.*121A=	NP_000259.1:n.*121A=
NM_016418.5:c.*181A= , LRG_511t2:c.*181A=	NP_057502.2:n.*181A=
NM_181828.2:c.*181A=	NP_861966.1:n.*181A=
NM_181829.2:c.*181A=	NP_861967.1:n.*181A=
NM_181830.2:c.*181A=	NP_861968.1:n.*181A=
NM_181832.2:c.*196A=	NP_861970.1:n.*196A=
NM_181833.2:c.*121A=	NP_861971.1:n.*121A=
NR_156186.1:n.2468A=
XM_017028809.2:c.*121A=	XP_016884298.1:n.*121A=
XM_017028810.1:c.*181A=	XP_016884299.1:n.*181A=
NM_000268.4:c.*121A= MANE Select	NP_000259.1:n.*121A=
NM_181828.3:c.*181A=	NP_861966.1:n.*181A=
NM_181829.3:c.*181A=	NP_861967.1:n.*181A=
NM_181830.3:c.*181A=	NP_861968.1:n.*181A=
NM_181832.3:c.*196A=	NP_861970.1:n.*196A=
NR_156186.2:n.2391A=
NM_181833.3:c.*121A=	NP_861971.1:n.*121A=