Canonical Allele Identifier: CA2400692322

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694852C= , CM000684.2:g.29694852C=	GRCh38
NC_000022.10:g.30090841C= , CM000684.1:g.30090841C=	GRCh37
NC_000022.9:g.28420841C=	NCBI36
NG_009057.1:g.96297C= , LRG_511:g.96297C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*50C=	ENSP00000354529.6:n.*50C=
ENST00000673312.2:c.*1332C=	ENSP00000500186.2:n.*1332C=
ENST00000338641.10:c.*50C= MANE Select	ENSP00000344666.5:n.*50C=
ENST00000361166.9:c.1256C=	ENSP00000354529.5:n.1256C=
ENST00000672461.1:c.*110C=	ENSP00000500919.1:n.*110C=
ENST00000672805.1:c.*1720C=	ENSP00000500295.1:n.*1720C=
ENST00000672896.1:c.*110C=	ENSP00000500117.1:n.*110C=
ENST00000673312.1:c.1857C=	ENSP00000500186.1:n.1857C=
ENST00000338641.8:c.*50C=	ENSP00000344666.4:n.*50C=
ENST00000361452.8:c.*110C=	ENSP00000354897.4:n.*110C=
ENST00000413209.6:c.*50C=	ENSP00000409921.2:n.*50C=
ENST00000432151.5:c.*194C=	ENSP00000395885.1:n.*194C=
NM_000268.3:c.*50C= , LRG_511t1:c.*50C=	NP_000259.1:n.*50C=
NM_016418.5:c.*110C= , LRG_511t2:c.*110C=	NP_057502.2:n.*110C=
NM_181828.2:c.*110C=	NP_861966.1:n.*110C=
NM_181829.2:c.*110C=	NP_861967.1:n.*110C=
NM_181830.2:c.*110C=	NP_861968.1:n.*110C=
NM_181832.2:c.*125C=	NP_861970.1:n.*125C=
NM_181833.2:c.*50C=	NP_861971.1:n.*50C=
NR_156186.1:n.2397C=
XM_017028809.2:c.*50C=	XP_016884298.1:n.*50C=
XM_017028810.1:c.*110C=	XP_016884299.1:n.*110C=
NM_000268.4:c.*50C= MANE Select	NP_000259.1:n.*50C=
NM_181828.3:c.*110C=	NP_861966.1:n.*110C=
NM_181829.3:c.*110C=	NP_861967.1:n.*110C=
NM_181830.3:c.*110C=	NP_861968.1:n.*110C=
NM_181832.3:c.*125C=	NP_861970.1:n.*125C=
NR_156186.2:n.2320C=
NM_181833.3:c.*50C=	NP_861971.1:n.*50C=