Canonical Allele Identifier: CA2400692320

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694850A= , CM000684.2:g.29694850A=	GRCh38
NC_000022.10:g.30090839A= , CM000684.1:g.30090839A=	GRCh37
NC_000022.9:g.28420839A=	NCBI36
NG_009057.1:g.96295A= , LRG_511:g.96295A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*48A=	ENSP00000354529.6:n.*48A=
ENST00000673312.2:c.*1330A=	ENSP00000500186.2:n.*1330A=
ENST00000338641.10:c.*48A= MANE Select	ENSP00000344666.5:n.*48A=
ENST00000361166.9:c.1254A=	ENSP00000354529.5:n.1254A=
ENST00000672461.1:c.*108A=	ENSP00000500919.1:n.*108A=
ENST00000672805.1:c.*1718A=	ENSP00000500295.1:n.*1718A=
ENST00000672896.1:c.*108A=	ENSP00000500117.1:n.*108A=
ENST00000673312.1:c.1855A=	ENSP00000500186.1:n.1855A=
ENST00000338641.8:c.*48A=	ENSP00000344666.4:n.*48A=
ENST00000361452.8:c.*108A=	ENSP00000354897.4:n.*108A=
ENST00000413209.6:c.*48A=	ENSP00000409921.2:n.*48A=
ENST00000432151.5:c.*192A=	ENSP00000395885.1:n.*192A=
NM_000268.3:c.*48A= , LRG_511t1:c.*48A=	NP_000259.1:n.*48A=
NM_016418.5:c.*108A= , LRG_511t2:c.*108A=	NP_057502.2:n.*108A=
NM_181828.2:c.*108A=	NP_861966.1:n.*108A=
NM_181829.2:c.*108A=	NP_861967.1:n.*108A=
NM_181830.2:c.*108A=	NP_861968.1:n.*108A=
NM_181832.2:c.*123A=	NP_861970.1:n.*123A=
NM_181833.2:c.*48A=	NP_861971.1:n.*48A=
NR_156186.1:n.2395A=
XM_017028809.2:c.*48A=	XP_016884298.1:n.*48A=
XM_017028810.1:c.*108A=	XP_016884299.1:n.*108A=
NM_000268.4:c.*48A= MANE Select	NP_000259.1:n.*48A=
NM_181828.3:c.*108A=	NP_861966.1:n.*108A=
NM_181829.3:c.*108A=	NP_861967.1:n.*108A=
NM_181830.3:c.*108A=	NP_861968.1:n.*108A=
NM_181832.3:c.*123A=	NP_861970.1:n.*123A=
NR_156186.2:n.2318A=
NM_181833.3:c.*48A=	NP_861971.1:n.*48A=