Canonical Allele Identifier: CA2400692333

Gene: NF2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.29694874G= , CM000684.2:g.29694874G=	GRCh38
NC_000022.10:g.30090863G= , CM000684.1:g.30090863G=	GRCh37
NC_000022.9:g.28420863G=	NCBI36
NG_009057.1:g.96319G= , LRG_511:g.96319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361166.10:c.*72G=	ENSP00000354529.6:n.*72G=
ENST00000673312.2:c.*1354G=	ENSP00000500186.2:n.*1354G=
ENST00000338641.10:c.*72G= MANE Select	ENSP00000344666.5:n.*72G=
ENST00000361166.9:c.1278G=	ENSP00000354529.5:n.1278G=
ENST00000672461.1:c.*132G=	ENSP00000500919.1:n.*132G=
ENST00000672805.1:c.*1742G=	ENSP00000500295.1:n.*1742G=
ENST00000672896.1:c.*132G=	ENSP00000500117.1:n.*132G=
ENST00000673312.1:c.1879G=	ENSP00000500186.1:n.1879G=
ENST00000338641.8:c.*72G=	ENSP00000344666.4:n.*72G=
ENST00000361452.8:c.*132G=	ENSP00000354897.4:n.*132G=
ENST00000413209.6:c.*72G=	ENSP00000409921.2:n.*72G=
ENST00000432151.5:c.*216G=	ENSP00000395885.1:n.*216G=
NM_000268.3:c.*72G= , LRG_511t1:c.*72G=	NP_000259.1:n.*72G=
NM_016418.5:c.*132G= , LRG_511t2:c.*132G=	NP_057502.2:n.*132G=
NM_181828.2:c.*132G=	NP_861966.1:n.*132G=
NM_181829.2:c.*132G=	NP_861967.1:n.*132G=
NM_181830.2:c.*132G=	NP_861968.1:n.*132G=
NM_181832.2:c.*147G=	NP_861970.1:n.*147G=
NM_181833.2:c.*72G=	NP_861971.1:n.*72G=
NR_156186.1:n.2419G=
XM_017028809.2:c.*72G=	XP_016884298.1:n.*72G=
XM_017028810.1:c.*132G=	XP_016884299.1:n.*132G=
NM_000268.4:c.*72G= MANE Select	NP_000259.1:n.*72G=
NM_181828.3:c.*132G=	NP_861966.1:n.*132G=
NM_181829.3:c.*132G=	NP_861967.1:n.*132G=
NM_181830.3:c.*132G=	NP_861968.1:n.*132G=
NM_181832.3:c.*147G=	NP_861970.1:n.*147G=
NR_156186.2:n.2342G=
NM_181833.3:c.*72G=	NP_861971.1:n.*72G=